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The Effects of Minocycline in Opioid-maintained Patients

The Effects of Minocycline on Opioid-induced Hyperalgesia in Opioid-Maintained Patients

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02359006
Enrollment
27
Registered
2015-02-09
Start date
2015-03-12
Completion date
2017-04-19
Last updated
2020-03-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Opioid Dependence, Pain

Keywords

Analgesia, pain analgesia, methadone, opiates

Brief summary

Opioids are the most commonly utilized pharmacological treatment for moderate to severe pain. However, their clinical value is hindered by the development of opioid-induced hyperalgesia (OIH). OIH manifests as heightened pain sensitivity, and is an increasingly challenging drawback to the efficacy of opioid treatment. Although the mechanism of action modulating OIH is not completely understood, previous animal studies suggest that this phenomenon is a result of proinflammatory responses. Thus, administering an adjunct anti-inflammatory agent may attenuate OIH. Minocycline is one such agent; it is a tetracycline derivative antibiotic that inhibits microglia activation, nitric oxide (NO) production, and the release of pro-inflammatory cytokines and chemokines. In fact, recent evidence suggests that minocycline may attenuate the neuroinflammatory effects of opioids while enhancing their antinociceptive effects. Therefore, the investigators will determine if minocycline will mitigate OIH in methadone-maintained patients.

Detailed description

Sixty completers will be recruited through the VA methadone clinic, as well as through the APT Foundation Methadone Maintenance Program. After the initial phone screening, potential subjects will undergo a comprehensive evaluation which will include medical, psychiatric, and drug use histories as well as physical, psychiatric, and laboratory examinations. Laboratory examination will include CBC, liver and thyroid function tests, serum electrolytes, BUN, creatinine, PT, PTT, urine analysis (including urine pregnancy for women) and urine toxicology screening. Participants will be terminated from the study following opioid relapse, or use of any other psychotropic medications. If participants are noncompliant (no-show, positive urine screening, noncompliance with medication protocol/missing more than one dose of minocycline/placebo), participation will be terminated. This double-blind, randomized clinical trial will randomize male and female veterans and non-veterans currently undergoing methadone maintenance treatment for opioid dependence to either minocycline (200mg/day) or placebo for 15 days. Upon inclusion, participants will be subjected to a pain assessment to evaluate baseline pain thresholds and tolerance: the Cold Pressor Test. An experimental treatment of either minocycline or placebo will then be initiated and maintained for 15 days. Additionally, at the beginning of Week 2 of treatment, participants will be given a Personal Digital Assistant (PDA) an HP iPAQ Pocket PC 2003 Pro that will administer Ecological Momentary Assessments (EMA). Using EMA, we can assess change in pain sensitivity, withdrawal symptoms and cognitive performance in the participants' natural environment, which increases the ecological validity of the study. Participants will be asked to return to the laboratory several times a week for the 15 consecutive days that they are taking minocycline in order to receive the study medication and to assess changes in pain thresholds and tolerance (i.e. to assess the presence, or lack thereof of hyperalgesia). Upon completion of experimental treatment, participants will be asked to return a final time to undergo pain measurement once more, to assess any changes in pain sensitivity after completion of minocycline.

Interventions

DRUGMinocycline

Minocycline will be compared with placebo

DRUGPlacebo

Placebo will be compared with minocycline

Sponsors

National Institute on Drug Abuse (NIDA)
CollaboratorNIH
Yale University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 55 Years
Healthy volunteers
No

Inclusion criteria

* Males and females, between the ages of 18 and 55 * Diagnosed with opioid dependence and currently enrolled in methadone maintenance treatment * Compliant in methadone maintenance treatment and on a stable dose for two weeks or greater * No current dependence or abuse of any other drugs (other than tobacco or marijuana) * No current medical problems * For women: * not pregnant as determined by pregnancy screening; * not breast feeding; u * using acceptable birth control methods; * not experiencing moderate to severe premenstrual symptoms (may interfere with pain assessment); * regular menstrual cycles

Exclusion criteria

* Current major psychiatric illnesses including mood, psychotic, or anxiety disorders * History of major medical illnesses, including liver diseases, heart disease, or other medical conditions that the physician investigator deems contraindicated for inclusion in the study * Current use of over-the-counter or prescription psychoactive drugs (including regular use of NSAIDS, antidepressant, anxiolytics, antipsychotics, mood stabilizers, psychostimulants) or drugs that would be expected to have major interactions with drugs to be tested, e.g., benzodiazepines, codeine, Percocet, and other opiate drugs * Liver function tests (ALT or AST) greater than 3x normal * Allergy to minocycline or other tetracyclines

Design outcomes

Primary

MeasureTime frameDescription
Pain ThresholdOne measurement at each of 5 weekly sessions: Baseline, Day 8, Day 15, Day 22 and at Follow-up (~Day 28)The Cold Pressor Test (CPT) measures pain threshold (in seconds). For this test, two water coolers filled with either warm (100.04ºF/37.8ºC) or cold water (32.9-34.7ºF/0.5-1.5ºC) are used. To begin the CPT, participants first immerse their hand into the warm-water bath for 2 min. Participants are then instructed to immerse their hand into the cold water bath and report the first time they experience pain (pain threshold). Lower scores indicate lower pain threshold. Minimum score is 0 seconds, and a maximum cut-off score of 300 seconds is used to prevent tissue damage.
Pain ToleranceOne measurement at each of 5 weekly sessions: Baseline, Day 8, Day 15, Day 22 and at Follow-up (~Day 28)The Cold Pressor Test (CPT) measures pain threshold and pain tolerance (in seconds). For this test, two water coolers filled with either warm (100.04ºF/37.8ºC) or cold water (32.9-34.7ºF/0.5-1.5ºC) are used. To begin the CPT, participants first immerse their hand into the warm-water bath for 2 min. Participants are then instructed to immerse their hand into the cold water bath and report when the pain becomes unbearable (pain tolerance). Lower scores indicate lower pain tolerance. Minimum score is 0 seconds, and a maximum cut-off score of 300 seconds is used to prevent tissue damage.

Secondary

MeasureTime frameDescription
Opioid Withdrawal Symptom Checklist (OWSC): Back Pain ItemOne measurement at each of 5 weekly sessions: Baseline, Day 8, Day 15, Day 22 and at Follow-up (~Day 28)For safety reasons, withdrawal signs and symptoms were assessed using a 22-item withdrawal instrument that has been reliably used to assess opiate withdrawal. As an additional assessment of daily pain, the presence of back pain item was analyzed. This item has a minimum score of 0 and maximum score of 4, with higher scores indicates more agreement with statement/more back pain.
Brief Pain Inventory - Short Form: Pain SeverityOne measurement at each of 5 weekly sessions: Baseline, Day 8, Day 15, Day 22 and at Follow-up (~Day 28)Brief Pain Inventory - Short Form: BPI-SF is a self-report questionnaire that assesses the impact of pain on daily function, location of pain, pain medications, and amount of pain relief in the past 24 hours or the past week. Each question is scored 0-10, and the scores are summed and then averaged to create a pain severity score. Minimum score is 0; maximum score is 10. Higher scores indicate more severely perceived pain.
Brief Pain Inventory - Short Form: InterferenceOne measurement at each of 5 weekly sessions: Baseline, Day 8, Day 15, Day 22 and at Follow-up (~Day 28)Brief Pain Inventory - Short Form: BPI-SF is a self-report questionnaire that assesses 7 questions each rated on a scale of 0-10, which are added and divided by 7. This average score of 7 questions gives a pain interference with living score, with a minimum score of 0 and a maximum score of 10. Higher scores indicate that pain interferes more with aspects of daily life.
Profile of Mood States (POMS) Depression SubscaleOne measurement at each of 5 weekly sessions: Baseline, Day 8, Day 15, Day 22 and at Follow-up (~Day 28)The POMS is a 65-item scale that divides items amongst eight mood states (tension, depression, anger, fatigue, confusion, vigor) on a 5-point rating scale (0=not at all to 5=extremely). We analyzed the 15-item Depression subscale, which has a minimum score of 0 and a maximum score of 75. Higher score indicate more agreement with the statement/more feelings of depression.
Profile of Mood States (POMS) - Total Mood DisturbanceOne measurement at each of 5 weekly sessions: Baseline, Day 8, Day 15, Day 22 and at Follow-up (~Day 28)The POMS is a 65-item scale that divides items amongst eight mood states (tension, depression, anger, fatigue, confusion, vigor) on a 5-point rating scale (0=not at all to 5=extremely). Total Mood Disturbance is calculated by adding the tension, depression, anger, fatigue, and confusion subscale scores and subtracting the vigor subscale score. This has a minimum of 0 and a maximum score of 210. Higher score indicate more mood disturbance.
Short-Form McGill Pain Questionnaire (SF-MPQ): Sensory SubscaleOne measurement at each of 5 weekly sessions: Baseline, Day 8, Day 15, Day 22 and at Follow-up (~Day 28)This measure is a subscale of the SF-MPQ, comprised of 11 of the 15 total items. The measure is completed immediately after the CPT, where participants describe their experience of CPT pain by choosing among a series of possible answers \[none (score=0), mild (score=1), moderate (score=2), or severe (score=3)\]. The items to describe the pain are 'Throbbing','Shooting', 'Stabbing', 'Sharp', 'Cramping', 'Gnawing', 'Hot/burning', 'Aching', 'Heavy', 'Tender', and 'Splitting'. The scores for these 11 items are summed as a measure of Sensory pain, with a minimum score of 0 and a maximum score of 33.
Short-Form McGill Pain Questionnaire (SF-MPQ): Affective SubscaleOne measurement at each of 5 weekly sessions: Baseline, Day 8, Day 15, Day 22 and at Follow-up (~Day 28)This measure is a subscale of the SF-MPQ, comprised of 4 of the 15 total items. The measure is completed immediately after the CPT, where participants describe their experience of CPT pain by choosing among a series of possible answers \[none (score=0), mild (score=1), moderate (score=2), or severe (score=3)\]. The items to describe the pain are 'Tiring-Exhausting', 'Sickening', 'Fearful', 'Punishing-Cruel'. The scores for these 4 items are summed as a measure of Affective pain, with a minimum score of 0 and a maximum score of 12.
Interleukin-1 Beta (IL-1β)Pre/post : At Screening before medication, and on Day 22 of medicationSerum cytokine analysis assayed using electrochemiluminescence multi-array technology (Meso Scale Discovery, Gaithersburg, MD). IL-1β is measured in pictograms per milliliter (pg/ml). Cytokines were assessed at screening (approximately 1 week prior to medication), and on the last day of medication treatment. Higher numbers indicate higher blood levels of this cytokine.
Interleukin-6 (IL-6)Pre/post : At Screening before medication, and on Day 22 of medicationSerum cytokine analysis assayed using electrochemiluminescence multi-array technology (Meso Scale Discovery, Gaithersburg, MD). IL-6 is measured in pictograms per milliliter (pg/ml).Cytokines were assessed at screening (approximately 1 week prior to medication), and on the last day of medication treatment. Higher numbers indicate higher blood levels of this cytokine.
Tumor Necrosis Factor Alpha (TNF-α)Pre/post : At Screening before medication, and on Day 22 of medicationSerum cytokine analysis assayed using electrochemiluminescence multi-array technology (Meso Scale Discovery, Gaithersburg, MD). TNF-α is measured in pictograms per milliliter (pg/ml).Cytokines were assessed at screening (approximately 1 week prior to medication), and on the last day of medication treatment. Higher numbers indicate higher blood levels of this cytokine.
Ecological Momentary Assessments (EMA) - Pain4x/day for one weekParticipants will be asked Do you feel any pain at this moment on seven-point Likert scales (1=strongly disagree to 7=strongly agree) 4 times per day outside of the laboratory (in their natural environment) using a personal digital assistant on days 8-14 of medication treatment. All scores were averaged to compute one score. Higher scores indicate more feelings of pain.
Ecological Momentary Assessments (EMA) - Craving4x/day for one weekParticipants will be asked Are you craving heroin at this moment on seven-point Likert scales (1=strongly disagree to 7=strongly agree) 4 times per day outside of the laboratory (in their natural environment) using a personal digital assistant on days 8-14 of medication treatment. All scores were averaged to compute one score. Higher scores indicate more craving for heroin.
Ecological Momentary Assessments (EMA): SOWS4x/day over one weekSelf-report opioid withdrawal scale. Withdrawal symptoms are measured on a 7-point Likert scale (1=strongly disagree, 7=strongly agree). Participants complete these ratings 4 times per day on days 8-14 of medication treatment. All scores were averaged to compute one score. Higher scores indicate more withdrawal symptoms.
Digit Symbol Substitution TestBaseline (Day 0), Pre- and 1-hour post-medication treatment on Test Days 8, 15 and 22, and at Follow-up (~Day 28The DSST is a test of psychomotor performance, which measures motor persistence, sustained attention, response speed and visuomotor coordination. The task is to fill in blank spaces with the symbols that are paired with the number above the blank space as fast as possible for 90 sec. The minimum score is 0 and the maximum score is 120. Higher numbers indicate better cognitive performance.
Sustained Attention to Response Test (SART): No-go Trials: Errors of CommissionBaseline (Day 0), Pre- and 1-hour post-medication treatment on Test Days 8, 15 and 22, and at Follow-up (~Day 28The SART is a Go No-Go task. It assesses the ability to withhold responses to an infrequently occurring target (No-Go trials). A total of 225 single digits (25 x 9 digits) are presented on a computer monitor for 250 ms each, immediately followed by a mask for 900 ms. Subjects must press a spacebar in response to every digit except the 3. Higher numbers indicate more errors of commission.
Sustained Attention to Response Test (SART): Go Trials: Errors of OmissionBaseline (Day 0), Pre- and 1-hour post-medication treatment on Test Days 8, 15 and 22, and at Follow-up (~Day 28The SART is a Go No-Go task. It assesses the ability to withhold responses to an infrequently occurring target (No-Go trials).The SART is a Go No-Go task. It assesses the ability to withhold responses to an infrequently occurring target (No-Go trials). A total of 225 single digits (25 x 9 digits) are presented on a computer monitor for 250 ms each, immediately followed by a mask for 900 ms. Subjects must press a spacebar in response to every digit except the 3. Higher numbers indicate more errors of omission.

Countries

United States

Participant flow

Recruitment details

Fifty-five subjects were screened. Of those, 27 were deemed eligible and enrolled.

Participants by arm

ArmCount
Minocycline
200mg minocycline Minocycline: Minocycline will be compared with placebo
10
Placebo
Sugar pill Placebo: Placebo will be compared with minocycline
10
Total20

Baseline characteristics

CharacteristicMinocyclinePlaceboTotal
Age, Continuous46.5 years
STANDARD_DEVIATION 4.5
47.9 years
STANDARD_DEVIATION 10
47.2 years
STANDARD_DEVIATION 7.59
Race/Ethnicity, Customized
Race/Ethnicity
Black
1 Participants2 Participants3 Participants
Race/Ethnicity, Customized
Race/Ethnicity
Hispanic
2 Participants1 Participants3 Participants
Race/Ethnicity, Customized
Race/Ethnicity
Other
0 Participants1 Participants1 Participants
Race/Ethnicity, Customized
Race/Ethnicity
White
7 Participants6 Participants13 Participants
Region of Enrollment
United States
10 participants10 participants20 participants
Sex: Female, Male
Female
3 Participants2 Participants5 Participants
Sex: Female, Male
Male
7 Participants8 Participants15 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 100 / 10
other
Total, other adverse events
0 / 100 / 10
serious
Total, serious adverse events
0 / 100 / 10

Outcome results

Primary

Pain Threshold

The Cold Pressor Test (CPT) measures pain threshold (in seconds). For this test, two water coolers filled with either warm (100.04ºF/37.8ºC) or cold water (32.9-34.7ºF/0.5-1.5ºC) are used. To begin the CPT, participants first immerse their hand into the warm-water bath for 2 min. Participants are then instructed to immerse their hand into the cold water bath and report the first time they experience pain (pain threshold). Lower scores indicate lower pain threshold. Minimum score is 0 seconds, and a maximum cut-off score of 300 seconds is used to prevent tissue damage.

Time frame: One measurement at each of 5 weekly sessions: Baseline, Day 8, Day 15, Day 22 and at Follow-up (~Day 28)

ArmMeasureGroupValue (MEAN)Dispersion
MinocyclinePain ThresholdDay 8 (Test Day 1)16.16 secondsStandard Deviation 6.46
MinocyclinePain ThresholdDay 22 (Test Day 3)16.21 secondsStandard Deviation 5.86
MinocyclinePain ThresholdDay 15 (Test Day 2)16.13 secondsStandard Deviation 5.67
MinocyclinePain Threshold~Day 28 (Follow-up)17.59 secondsStandard Deviation 9.34
MinocyclinePain ThresholdBaseline18.72 secondsStandard Deviation 11.25
PlaceboPain Threshold~Day 28 (Follow-up)21.92 secondsStandard Deviation 7.93
PlaceboPain ThresholdBaseline24.78 secondsStandard Deviation 13.77
PlaceboPain ThresholdDay 8 (Test Day 1)24.37 secondsStandard Deviation 17.57
PlaceboPain ThresholdDay 15 (Test Day 2)18.46 secondsStandard Deviation 6.86
PlaceboPain ThresholdDay 22 (Test Day 3)25.75 secondsStandard Deviation 15.45
Primary

Pain Tolerance

The Cold Pressor Test (CPT) measures pain threshold and pain tolerance (in seconds). For this test, two water coolers filled with either warm (100.04ºF/37.8ºC) or cold water (32.9-34.7ºF/0.5-1.5ºC) are used. To begin the CPT, participants first immerse their hand into the warm-water bath for 2 min. Participants are then instructed to immerse their hand into the cold water bath and report when the pain becomes unbearable (pain tolerance). Lower scores indicate lower pain tolerance. Minimum score is 0 seconds, and a maximum cut-off score of 300 seconds is used to prevent tissue damage.

Time frame: One measurement at each of 5 weekly sessions: Baseline, Day 8, Day 15, Day 22 and at Follow-up (~Day 28)

ArmMeasureGroupValue (MEAN)Dispersion
MinocyclinePain ToleranceDay 8 (Test Day 1)37.42 secondsStandard Deviation 12.76
MinocyclinePain ToleranceDay 22 (Test Day 3)36.61 secondsStandard Deviation 20.45
MinocyclinePain ToleranceDay 15 (Test Day 2)34.41 secondsStandard Deviation 11.84
MinocyclinePain Tolerance~Day 28 (Follow-up)31.58 secondsStandard Deviation 12.56
MinocyclinePain ToleranceBaseline40.86 secondsStandard Deviation 21.71
PlaceboPain Tolerance~Day 28 (Follow-up)43.14 secondsStandard Deviation 15.46
PlaceboPain ToleranceBaseline59.72 secondsStandard Deviation 30.4
PlaceboPain ToleranceDay 8 (Test Day 1)52.56 secondsStandard Deviation 28.54
PlaceboPain ToleranceDay 15 (Test Day 2)48.42 secondsStandard Deviation 36.62
PlaceboPain ToleranceDay 22 (Test Day 3)51.52 secondsStandard Deviation 37.53
Secondary

Brief Pain Inventory - Short Form: Interference

Brief Pain Inventory - Short Form: BPI-SF is a self-report questionnaire that assesses 7 questions each rated on a scale of 0-10, which are added and divided by 7. This average score of 7 questions gives a pain interference with living score, with a minimum score of 0 and a maximum score of 10. Higher scores indicate that pain interferes more with aspects of daily life.

Time frame: One measurement at each of 5 weekly sessions: Baseline, Day 8, Day 15, Day 22 and at Follow-up (~Day 28)

ArmMeasureGroupValue (MEAN)Dispersion
MinocyclineBrief Pain Inventory - Short Form: InterferenceDay 8 (Test Day 1)0.90 score on a scaleStandard Deviation 1.69
MinocyclineBrief Pain Inventory - Short Form: InterferenceDay 22 (Test Day 3)0.67 score on a scaleStandard Deviation 1.3
MinocyclineBrief Pain Inventory - Short Form: InterferenceDay 15 (Test Day 2)0.63 score on a scaleStandard Deviation 1.23
MinocyclineBrief Pain Inventory - Short Form: Interference~Day 28 (Follow-up)0.52 score on a scaleStandard Deviation 0.89
MinocyclineBrief Pain Inventory - Short Form: InterferenceBaseline0.93 score on a scaleStandard Deviation 1.74
PlaceboBrief Pain Inventory - Short Form: Interference~Day 28 (Follow-up)1.2 score on a scaleStandard Deviation 2.57
PlaceboBrief Pain Inventory - Short Form: InterferenceBaseline0.97 score on a scaleStandard Deviation 2.37
PlaceboBrief Pain Inventory - Short Form: InterferenceDay 8 (Test Day 1)1.33 score on a scaleStandard Deviation 2.07
PlaceboBrief Pain Inventory - Short Form: InterferenceDay 15 (Test Day 2)1.04 score on a scaleStandard Deviation 2.15
PlaceboBrief Pain Inventory - Short Form: InterferenceDay 22 (Test Day 3)1.49 score on a scaleStandard Deviation 2.57
Secondary

Brief Pain Inventory - Short Form: Pain Severity

Brief Pain Inventory - Short Form: BPI-SF is a self-report questionnaire that assesses the impact of pain on daily function, location of pain, pain medications, and amount of pain relief in the past 24 hours or the past week. Each question is scored 0-10, and the scores are summed and then averaged to create a pain severity score. Minimum score is 0; maximum score is 10. Higher scores indicate more severely perceived pain.

Time frame: One measurement at each of 5 weekly sessions: Baseline, Day 8, Day 15, Day 22 and at Follow-up (~Day 28)

ArmMeasureGroupValue (MEAN)Dispersion
MinocyclineBrief Pain Inventory - Short Form: Pain SeverityDay 8 (Test Day 1)0.88 score on a scaleStandard Deviation 1.56
MinocyclineBrief Pain Inventory - Short Form: Pain SeverityDay 22 (Test Day 3)0.80 score on a scaleStandard Deviation 1.3
MinocyclineBrief Pain Inventory - Short Form: Pain SeverityDay 15 (Test Day 2)0.78 score on a scaleStandard Deviation 1.27
MinocyclineBrief Pain Inventory - Short Form: Pain Severity~Day 28 (Follow-up)1.10 score on a scaleStandard Deviation 1.45
MinocyclineBrief Pain Inventory - Short Form: Pain SeverityBaseline1.28 score on a scaleStandard Deviation 1.83
PlaceboBrief Pain Inventory - Short Form: Pain Severity~Day 28 (Follow-up)1.28 score on a scaleStandard Deviation 2.57
PlaceboBrief Pain Inventory - Short Form: Pain SeverityBaseline1.10 score on a scaleStandard Deviation 1.93
PlaceboBrief Pain Inventory - Short Form: Pain SeverityDay 8 (Test Day 1)0.95 score on a scaleStandard Deviation 1.96
PlaceboBrief Pain Inventory - Short Form: Pain SeverityDay 15 (Test Day 2)1.00 score on a scaleStandard Deviation 1.81
PlaceboBrief Pain Inventory - Short Form: Pain SeverityDay 22 (Test Day 3)1.18 score on a scaleStandard Deviation 2.66
Secondary

Digit Symbol Substitution Test

The DSST is a test of psychomotor performance, which measures motor persistence, sustained attention, response speed and visuomotor coordination. The task is to fill in blank spaces with the symbols that are paired with the number above the blank space as fast as possible for 90 sec. The minimum score is 0 and the maximum score is 120. Higher numbers indicate better cognitive performance.

Time frame: Baseline (Day 0), Pre- and 1-hour post-medication treatment on Test Days 8, 15 and 22, and at Follow-up (~Day 28

ArmMeasureGroupValue (MEAN)Dispersion
MinocyclineDigit Symbol Substitution TestDay 8 Post-medication41.78 score on a scaleStandard Deviation 6.72
MinocyclineDigit Symbol Substitution TestBaseline37.11 score on a scaleStandard Deviation 8.57
MinocyclineDigit Symbol Substitution TestDay 8 Pre-medication42.33 score on a scaleStandard Deviation 8.12
MinocyclineDigit Symbol Substitution TestDay 15 Pre-medication45.67 score on a scaleStandard Deviation 8.32
MinocyclineDigit Symbol Substitution TestDay 15 Post-medication43.25 score on a scaleStandard Deviation 11.51
MinocyclineDigit Symbol Substitution TestDay 22 Pre-medication48.44 score on a scaleStandard Deviation 13.38
MinocyclineDigit Symbol Substitution TestDay 22 Post-medication46.56 score on a scaleStandard Deviation 9.19
MinocyclineDigit Symbol Substitution Test~Day 28 (Follow-up)50.75 score on a scaleStandard Deviation 8.97
PlaceboDigit Symbol Substitution Test~Day 28 (Follow-up)46.67 score on a scaleStandard Deviation 5.89
PlaceboDigit Symbol Substitution TestDay 15 Post-medication41.11 score on a scaleStandard Deviation 7.41
PlaceboDigit Symbol Substitution TestBaseline37.11 score on a scaleStandard Deviation 9.05
PlaceboDigit Symbol Substitution TestDay 22 Post-medication40.11 score on a scaleStandard Deviation 9.16
PlaceboDigit Symbol Substitution TestDay 8 Pre-medication40.89 score on a scaleStandard Deviation 4.96
PlaceboDigit Symbol Substitution TestDay 8 Post-medication40.89 score on a scaleStandard Deviation 5.3
PlaceboDigit Symbol Substitution TestDay 22 Pre-medication43.00 score on a scaleStandard Deviation 7.23
PlaceboDigit Symbol Substitution TestDay 15 Pre-medication43.33 score on a scaleStandard Deviation 6.96
Secondary

Ecological Momentary Assessments (EMA) - Craving

Participants will be asked Are you craving heroin at this moment on seven-point Likert scales (1=strongly disagree to 7=strongly agree) 4 times per day outside of the laboratory (in their natural environment) using a personal digital assistant on days 8-14 of medication treatment. All scores were averaged to compute one score. Higher scores indicate more craving for heroin.

Time frame: 4x/day for one week

ArmMeasureValue (MEAN)Dispersion
MinocyclineEcological Momentary Assessments (EMA) - Craving1.04 score on a scaleStandard Deviation 0.18
PlaceboEcological Momentary Assessments (EMA) - Craving1.14 score on a scaleStandard Deviation 0.49
Secondary

Ecological Momentary Assessments (EMA) - Pain

Participants will be asked Do you feel any pain at this moment on seven-point Likert scales (1=strongly disagree to 7=strongly agree) 4 times per day outside of the laboratory (in their natural environment) using a personal digital assistant on days 8-14 of medication treatment. All scores were averaged to compute one score. Higher scores indicate more feelings of pain.

Time frame: 4x/day for one week

ArmMeasureValue (MEAN)Dispersion
MinocyclineEcological Momentary Assessments (EMA) - Pain1.22 score on a scaleStandard Deviation 0.63
PlaceboEcological Momentary Assessments (EMA) - Pain1.14 score on a scaleStandard Deviation 0.49
Secondary

Ecological Momentary Assessments (EMA): SOWS

Self-report opioid withdrawal scale. Withdrawal symptoms are measured on a 7-point Likert scale (1=strongly disagree, 7=strongly agree). Participants complete these ratings 4 times per day on days 8-14 of medication treatment. All scores were averaged to compute one score. Higher scores indicate more withdrawal symptoms.

Time frame: 4x/day over one week

ArmMeasureValue (MEAN)Dispersion
MinocyclineEcological Momentary Assessments (EMA): SOWS1.05 score on a scaleStandard Deviation 0.24
PlaceboEcological Momentary Assessments (EMA): SOWS1.03 score on a scaleStandard Deviation 0.22
Secondary

Interleukin-1 Beta (IL-1β)

Serum cytokine analysis assayed using electrochemiluminescence multi-array technology (Meso Scale Discovery, Gaithersburg, MD). IL-1β is measured in pictograms per milliliter (pg/ml). Cytokines were assessed at screening (approximately 1 week prior to medication), and on the last day of medication treatment. Higher numbers indicate higher blood levels of this cytokine.

Time frame: Pre/post : At Screening before medication, and on Day 22 of medication

ArmMeasureGroupValue (MEAN)Dispersion
MinocyclineInterleukin-1 Beta (IL-1β)Screening0.80 pictograms per milliliterStandard Deviation 0.58
MinocyclineInterleukin-1 Beta (IL-1β)Day 220.67 pictograms per milliliterStandard Deviation 0.44
PlaceboInterleukin-1 Beta (IL-1β)Screening0.72 pictograms per milliliterStandard Deviation 0.55
PlaceboInterleukin-1 Beta (IL-1β)Day 220.62 pictograms per milliliterStandard Deviation 0.53
Secondary

Interleukin-6 (IL-6)

Serum cytokine analysis assayed using electrochemiluminescence multi-array technology (Meso Scale Discovery, Gaithersburg, MD). IL-6 is measured in pictograms per milliliter (pg/ml).Cytokines were assessed at screening (approximately 1 week prior to medication), and on the last day of medication treatment. Higher numbers indicate higher blood levels of this cytokine.

Time frame: Pre/post : At Screening before medication, and on Day 22 of medication

ArmMeasureGroupValue (MEAN)Dispersion
MinocyclineInterleukin-6 (IL-6)Screening1.64 pictograms per milliliterStandard Deviation 1.3
MinocyclineInterleukin-6 (IL-6)Day 222.14 pictograms per milliliterStandard Deviation 1.63
PlaceboInterleukin-6 (IL-6)Screening1.11 pictograms per milliliterStandard Deviation 0.94
PlaceboInterleukin-6 (IL-6)Day 221.99 pictograms per milliliterStandard Deviation 2.53
Secondary

Opioid Withdrawal Symptom Checklist (OWSC): Back Pain Item

For safety reasons, withdrawal signs and symptoms were assessed using a 22-item withdrawal instrument that has been reliably used to assess opiate withdrawal. As an additional assessment of daily pain, the presence of back pain item was analyzed. This item has a minimum score of 0 and maximum score of 4, with higher scores indicates more agreement with statement/more back pain.

Time frame: One measurement at each of 5 weekly sessions: Baseline, Day 8, Day 15, Day 22 and at Follow-up (~Day 28)

ArmMeasureGroupValue (MEAN)Dispersion
MinocyclineOpioid Withdrawal Symptom Checklist (OWSC): Back Pain ItemDay 8 (Test Day 1)0 score on a scaleStandard Deviation 0
MinocyclineOpioid Withdrawal Symptom Checklist (OWSC): Back Pain ItemDay 22 (Test Day 3)0.20 score on a scaleStandard Deviation 0.42
MinocyclineOpioid Withdrawal Symptom Checklist (OWSC): Back Pain ItemDay 15 (Test Day 2)0.10 score on a scaleStandard Deviation 0.32
MinocyclineOpioid Withdrawal Symptom Checklist (OWSC): Back Pain Item~Day 28 (Follow-up)0.10 score on a scaleStandard Deviation 0.32
MinocyclineOpioid Withdrawal Symptom Checklist (OWSC): Back Pain ItemBaseline0 score on a scaleStandard Deviation 0
PlaceboOpioid Withdrawal Symptom Checklist (OWSC): Back Pain Item~Day 28 (Follow-up)0.40 score on a scaleStandard Deviation 0.97
PlaceboOpioid Withdrawal Symptom Checklist (OWSC): Back Pain ItemBaseline0.10 score on a scaleStandard Deviation 0.32
PlaceboOpioid Withdrawal Symptom Checklist (OWSC): Back Pain ItemDay 8 (Test Day 1)0.10 score on a scaleStandard Deviation 0.7
PlaceboOpioid Withdrawal Symptom Checklist (OWSC): Back Pain ItemDay 15 (Test Day 2)0.20 score on a scaleStandard Deviation 0.63
PlaceboOpioid Withdrawal Symptom Checklist (OWSC): Back Pain ItemDay 22 (Test Day 3)0.20 score on a scaleStandard Deviation 0.63
Secondary

Profile of Mood States (POMS) Depression Subscale

The POMS is a 65-item scale that divides items amongst eight mood states (tension, depression, anger, fatigue, confusion, vigor) on a 5-point rating scale (0=not at all to 5=extremely). We analyzed the 15-item Depression subscale, which has a minimum score of 0 and a maximum score of 75. Higher score indicate more agreement with the statement/more feelings of depression.

Time frame: One measurement at each of 5 weekly sessions: Baseline, Day 8, Day 15, Day 22 and at Follow-up (~Day 28)

ArmMeasureGroupValue (MEAN)Dispersion
MinocyclineProfile of Mood States (POMS) Depression SubscaleDay 8 (Test Day 1)18.9 score on a scaleStandard Deviation 5.22
MinocyclineProfile of Mood States (POMS) Depression SubscaleDay 22 (Test Day 3)19.2 score on a scaleStandard Deviation 5.43
MinocyclineProfile of Mood States (POMS) Depression SubscaleBaseline20.80 score on a scaleStandard Deviation 5.33
MinocyclineProfile of Mood States (POMS) Depression Subscale~Day 28 (Follow-up)18.8 score on a scaleStandard Deviation 7.57
MinocyclineProfile of Mood States (POMS) Depression SubscaleDay 15 (Test Day 2)21.00 score on a scaleStandard Deviation 6.46
PlaceboProfile of Mood States (POMS) Depression Subscale~Day 28 (Follow-up)17.8 score on a scaleStandard Deviation 7.87
PlaceboProfile of Mood States (POMS) Depression SubscaleDay 8 (Test Day 1)17.9 score on a scaleStandard Deviation 3.35
PlaceboProfile of Mood States (POMS) Depression SubscaleDay 15 (Test Day 2)16.7 score on a scaleStandard Deviation 3.71
PlaceboProfile of Mood States (POMS) Depression SubscaleDay 22 (Test Day 3)17.0 score on a scaleStandard Deviation 5.01
PlaceboProfile of Mood States (POMS) Depression SubscaleBaseline18.9 score on a scaleStandard Deviation 5.22
Secondary

Profile of Mood States (POMS) - Total Mood Disturbance

The POMS is a 65-item scale that divides items amongst eight mood states (tension, depression, anger, fatigue, confusion, vigor) on a 5-point rating scale (0=not at all to 5=extremely). Total Mood Disturbance is calculated by adding the tension, depression, anger, fatigue, and confusion subscale scores and subtracting the vigor subscale score. This has a minimum of 0 and a maximum score of 210. Higher score indicate more mood disturbance.

Time frame: One measurement at each of 5 weekly sessions: Baseline, Day 8, Day 15, Day 22 and at Follow-up (~Day 28)

ArmMeasureGroupValue (MEAN)Dispersion
MinocyclineProfile of Mood States (POMS) - Total Mood DisturbanceDay 8 (Test Day 1)44.7 score on a scaleStandard Deviation 14.43
MinocyclineProfile of Mood States (POMS) - Total Mood DisturbanceDay 22 (Test Day 3)43.4 score on a scaleStandard Deviation 17.51
MinocyclineProfile of Mood States (POMS) - Total Mood DisturbanceBaseline43.1 score on a scaleStandard Deviation 15.04
MinocyclineProfile of Mood States (POMS) - Total Mood Disturbance~Day 28 (Follow-up)40.7 score on a scaleStandard Deviation 15.52
MinocyclineProfile of Mood States (POMS) - Total Mood DisturbanceDay 15 (Test Day 2)50.3 score on a scaleStandard Deviation 18.29
PlaceboProfile of Mood States (POMS) - Total Mood Disturbance~Day 28 (Follow-up)42.2 score on a scaleStandard Deviation 23.61
PlaceboProfile of Mood States (POMS) - Total Mood DisturbanceDay 8 (Test Day 1)41.88 score on a scaleStandard Deviation 13.62
PlaceboProfile of Mood States (POMS) - Total Mood DisturbanceDay 15 (Test Day 2)40.4 score on a scaleStandard Deviation 15.38
PlaceboProfile of Mood States (POMS) - Total Mood DisturbanceDay 22 (Test Day 3)42.3 score on a scaleStandard Deviation 17.51
PlaceboProfile of Mood States (POMS) - Total Mood DisturbanceBaseline47.4 score on a scaleStandard Deviation 22.63
Secondary

Short-Form McGill Pain Questionnaire (SF-MPQ): Affective Subscale

This measure is a subscale of the SF-MPQ, comprised of 4 of the 15 total items. The measure is completed immediately after the CPT, where participants describe their experience of CPT pain by choosing among a series of possible answers \[none (score=0), mild (score=1), moderate (score=2), or severe (score=3)\]. The items to describe the pain are 'Tiring-Exhausting', 'Sickening', 'Fearful', 'Punishing-Cruel'. The scores for these 4 items are summed as a measure of Affective pain, with a minimum score of 0 and a maximum score of 12.

Time frame: One measurement at each of 5 weekly sessions: Baseline, Day 8, Day 15, Day 22 and at Follow-up (~Day 28)

ArmMeasureGroupValue (MEAN)Dispersion
MinocyclineShort-Form McGill Pain Questionnaire (SF-MPQ): Affective SubscaleBaseline2.0 score on a scaleStandard Deviation 3.32
MinocyclineShort-Form McGill Pain Questionnaire (SF-MPQ): Affective SubscaleDay 15 (Test Day 2)1.9 score on a scaleStandard Deviation 3.45
MinocyclineShort-Form McGill Pain Questionnaire (SF-MPQ): Affective Subscale~Day 28 (Follow-up)1.89 score on a scaleStandard Deviation 3.48
MinocyclineShort-Form McGill Pain Questionnaire (SF-MPQ): Affective SubscaleDay 22 (Test Day 3)2.4 score on a scaleStandard Deviation 3.24
MinocyclineShort-Form McGill Pain Questionnaire (SF-MPQ): Affective SubscaleDay 8 (Test Day 1)1.7 score on a scaleStandard Deviation 2.11
PlaceboShort-Form McGill Pain Questionnaire (SF-MPQ): Affective Subscale~Day 28 (Follow-up)2.3 score on a scaleStandard Deviation 4.22
PlaceboShort-Form McGill Pain Questionnaire (SF-MPQ): Affective SubscaleBaseline1.5 score on a scaleStandard Deviation 2.22
PlaceboShort-Form McGill Pain Questionnaire (SF-MPQ): Affective SubscaleDay 8 (Test Day 1)1.7 score on a scaleStandard Deviation 2.11
PlaceboShort-Form McGill Pain Questionnaire (SF-MPQ): Affective SubscaleDay 15 (Test Day 2)2.2 score on a scaleStandard Deviation 3.74
PlaceboShort-Form McGill Pain Questionnaire (SF-MPQ): Affective SubscaleDay 22 (Test Day 3)2.0 score on a scaleStandard Deviation 3.74
Secondary

Short-Form McGill Pain Questionnaire (SF-MPQ): Sensory Subscale

This measure is a subscale of the SF-MPQ, comprised of 11 of the 15 total items. The measure is completed immediately after the CPT, where participants describe their experience of CPT pain by choosing among a series of possible answers \[none (score=0), mild (score=1), moderate (score=2), or severe (score=3)\]. The items to describe the pain are 'Throbbing','Shooting', 'Stabbing', 'Sharp', 'Cramping', 'Gnawing', 'Hot/burning', 'Aching', 'Heavy', 'Tender', and 'Splitting'. The scores for these 11 items are summed as a measure of Sensory pain, with a minimum score of 0 and a maximum score of 33.

Time frame: One measurement at each of 5 weekly sessions: Baseline, Day 8, Day 15, Day 22 and at Follow-up (~Day 28)

ArmMeasureGroupValue (MEAN)Dispersion
MinocyclineShort-Form McGill Pain Questionnaire (SF-MPQ): Sensory SubscaleDay 8 (Test Day 1)10.9 score on a scaleStandard Deviation 8.32
MinocyclineShort-Form McGill Pain Questionnaire (SF-MPQ): Sensory SubscaleDay 22 (Test Day 3)11.3 score on a scaleStandard Deviation 8.26
MinocyclineShort-Form McGill Pain Questionnaire (SF-MPQ): Sensory SubscaleDay 15 (Test Day 2)10.8 score on a scaleStandard Deviation 7.54
MinocyclineShort-Form McGill Pain Questionnaire (SF-MPQ): Sensory Subscale~Day 28 (Follow-up)12.5 score on a scaleStandard Deviation 7.8
MinocyclineShort-Form McGill Pain Questionnaire (SF-MPQ): Sensory SubscaleBaseline10.33 score on a scaleStandard Deviation 7.88
PlaceboShort-Form McGill Pain Questionnaire (SF-MPQ): Sensory Subscale~Day 28 (Follow-up)10.7 score on a scaleStandard Deviation 8.82
PlaceboShort-Form McGill Pain Questionnaire (SF-MPQ): Sensory SubscaleBaseline12.9 score on a scaleStandard Deviation 8.69
PlaceboShort-Form McGill Pain Questionnaire (SF-MPQ): Sensory SubscaleDay 8 (Test Day 1)13.1 score on a scaleStandard Deviation 4.77
PlaceboShort-Form McGill Pain Questionnaire (SF-MPQ): Sensory SubscaleDay 15 (Test Day 2)14.2 score on a scaleStandard Deviation 11.05
PlaceboShort-Form McGill Pain Questionnaire (SF-MPQ): Sensory SubscaleDay 22 (Test Day 3)13.3 score on a scaleStandard Deviation 9.44
Secondary

Sustained Attention to Response Test (SART): Go Trials: Errors of Omission

The SART is a Go No-Go task. It assesses the ability to withhold responses to an infrequently occurring target (No-Go trials).The SART is a Go No-Go task. It assesses the ability to withhold responses to an infrequently occurring target (No-Go trials). A total of 225 single digits (25 x 9 digits) are presented on a computer monitor for 250 ms each, immediately followed by a mask for 900 ms. Subjects must press a spacebar in response to every digit except the 3. Higher numbers indicate more errors of omission.

Time frame: Baseline (Day 0), Pre- and 1-hour post-medication treatment on Test Days 8, 15 and 22, and at Follow-up (~Day 28

ArmMeasureGroupValue (MEAN)Dispersion
MinocyclineSustained Attention to Response Test (SART): Go Trials: Errors of OmissionBaseline10.9 ommission errorsStandard Deviation 8.17
MinocyclineSustained Attention to Response Test (SART): Go Trials: Errors of OmissionDay 15 Post-medication7.7 ommission errorsStandard Deviation 12.14
MinocyclineSustained Attention to Response Test (SART): Go Trials: Errors of OmissionDay 22 Pre-medication18.4 ommission errorsStandard Deviation 18.71
MinocyclineSustained Attention to Response Test (SART): Go Trials: Errors of OmissionDay 8 Post-medication6.88 ommission errorsStandard Deviation 8.08
MinocyclineSustained Attention to Response Test (SART): Go Trials: Errors of OmissionDay 22 Post-medication13.2 ommission errorsStandard Deviation 12.22
MinocyclineSustained Attention to Response Test (SART): Go Trials: Errors of OmissionDay 8 Pre-medication9.11 ommission errorsStandard Deviation 12.67
MinocyclineSustained Attention to Response Test (SART): Go Trials: Errors of Omission~Day 28 (Follow-up)11.1 ommission errorsStandard Deviation 7.69
MinocyclineSustained Attention to Response Test (SART): Go Trials: Errors of OmissionDay 15 Pre-medication15.8 ommission errorsStandard Deviation 29.67
PlaceboSustained Attention to Response Test (SART): Go Trials: Errors of Omission~Day 28 (Follow-up)21.1 ommission errorsStandard Deviation 21.13
PlaceboSustained Attention to Response Test (SART): Go Trials: Errors of OmissionDay 15 Post-medication27 ommission errorsStandard Deviation 27.87
PlaceboSustained Attention to Response Test (SART): Go Trials: Errors of OmissionBaseline17.9 ommission errorsStandard Deviation 16.78
PlaceboSustained Attention to Response Test (SART): Go Trials: Errors of OmissionDay 8 Pre-medication13.78 ommission errorsStandard Deviation 9.93
PlaceboSustained Attention to Response Test (SART): Go Trials: Errors of OmissionDay 8 Post-medication13.44 ommission errorsStandard Deviation 9.94
PlaceboSustained Attention to Response Test (SART): Go Trials: Errors of OmissionDay 15 Pre-medication21 ommission errorsStandard Deviation 23.81
PlaceboSustained Attention to Response Test (SART): Go Trials: Errors of OmissionDay 22 Pre-medication25.4 ommission errorsStandard Deviation 30.16
PlaceboSustained Attention to Response Test (SART): Go Trials: Errors of OmissionDay 22 Post-medication22.33 ommission errorsStandard Deviation 24.79
Secondary

Sustained Attention to Response Test (SART): No-go Trials: Errors of Commission

The SART is a Go No-Go task. It assesses the ability to withhold responses to an infrequently occurring target (No-Go trials). A total of 225 single digits (25 x 9 digits) are presented on a computer monitor for 250 ms each, immediately followed by a mask for 900 ms. Subjects must press a spacebar in response to every digit except the 3. Higher numbers indicate more errors of commission.

Time frame: Baseline (Day 0), Pre- and 1-hour post-medication treatment on Test Days 8, 15 and 22, and at Follow-up (~Day 28

ArmMeasureGroupValue (MEAN)Dispersion
MinocyclineSustained Attention to Response Test (SART): No-go Trials: Errors of CommissionBaseline7 commission errorsStandard Deviation 6.41
MinocyclineSustained Attention to Response Test (SART): No-go Trials: Errors of CommissionDay 15 Post-medication5.5 commission errorsStandard Deviation 5.8
MinocyclineSustained Attention to Response Test (SART): No-go Trials: Errors of CommissionDay 8 Post-medication5.75 commission errorsStandard Deviation 5.09
MinocyclineSustained Attention to Response Test (SART): No-go Trials: Errors of CommissionDay 22 Pre-medication9.3 commission errorsStandard Deviation 5.58
MinocyclineSustained Attention to Response Test (SART): No-go Trials: Errors of CommissionDay 8 Pre-medication5.78 commission errorsStandard Deviation 4.6
MinocyclineSustained Attention to Response Test (SART): No-go Trials: Errors of CommissionDay 15 Pre-medication7.40 commission errorsStandard Deviation 5.76
MinocyclineSustained Attention to Response Test (SART): No-go Trials: Errors of Commission~Day 28 (Follow-up)7.00 commission errorsStandard Deviation 4.54
MinocyclineSustained Attention to Response Test (SART): No-go Trials: Errors of CommissionDay 22 Post-medication5.6 commission errorsStandard Deviation 4.78
PlaceboSustained Attention to Response Test (SART): No-go Trials: Errors of Commission~Day 28 (Follow-up)7.26 commission errorsStandard Deviation 6.88
PlaceboSustained Attention to Response Test (SART): No-go Trials: Errors of CommissionBaseline9 commission errorsStandard Deviation 5.4
PlaceboSustained Attention to Response Test (SART): No-go Trials: Errors of CommissionDay 8 Pre-medication8.33 commission errorsStandard Deviation 6.16
PlaceboSustained Attention to Response Test (SART): No-go Trials: Errors of CommissionDay 8 Post-medication7.33 commission errorsStandard Deviation 5.27
PlaceboSustained Attention to Response Test (SART): No-go Trials: Errors of CommissionDay 15 Pre-medication7.89 commission errorsStandard Deviation 6.47
PlaceboSustained Attention to Response Test (SART): No-go Trials: Errors of CommissionDay 15 Post-medication8.7 commission errorsStandard Deviation 5.1
PlaceboSustained Attention to Response Test (SART): No-go Trials: Errors of CommissionDay 22 Pre-medication7.3 commission errorsStandard Deviation 7.67
PlaceboSustained Attention to Response Test (SART): No-go Trials: Errors of CommissionDay 22 Post-medication9.89 commission errorsStandard Deviation 7.27
Secondary

Tumor Necrosis Factor Alpha (TNF-α)

Serum cytokine analysis assayed using electrochemiluminescence multi-array technology (Meso Scale Discovery, Gaithersburg, MD). TNF-α is measured in pictograms per milliliter (pg/ml).Cytokines were assessed at screening (approximately 1 week prior to medication), and on the last day of medication treatment. Higher numbers indicate higher blood levels of this cytokine.

Time frame: Pre/post : At Screening before medication, and on Day 22 of medication

ArmMeasureGroupValue (MEAN)Dispersion
MinocyclineTumor Necrosis Factor Alpha (TNF-α)Screening2.86 pictograms per milliliterStandard Deviation 1.79
MinocyclineTumor Necrosis Factor Alpha (TNF-α)Day 222.66 pictograms per milliliterStandard Deviation 0.8
PlaceboTumor Necrosis Factor Alpha (TNF-α)Screening2.66 pictograms per milliliterStandard Deviation 0.8
PlaceboTumor Necrosis Factor Alpha (TNF-α)Day 222.53 pictograms per milliliterStandard Deviation 0.96

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026