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Buprenorphine and Methadone for Opioid-dependent Chronic Back Pain Patients

A Randomized Controlled Trial Comparing Buprenorphine and Methadone for Treatment in Opioid Dependent Chronic Back Pain Patients

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01559454
Enrollment
19
Registered
2012-03-21
Start date
2012-02-29
Completion date
2014-05-31
Last updated
2020-11-03

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

Conditions

Low Back Pain

Keywords

chronic pain, opioid dependence, methadone, buprenorphine, substance use disorder

Brief summary

Chronic pain patients are treated with prescription opioids and many exhibit opioid addiction. Currently, there are no evidence-based guidelines to better manage patients with chronic pain and coexistent opioid addiction. This study compares 6-months buprenorphine and methadone treatment in these patients. The investigators hypothesize that both buprenorphine and methadone treatment will reduce pain and addiction behaviors and increase functioning in these patients.

Detailed description

Chronic non-malignant pain (i.e. pain unrelated to cancer that persists beyond the usual course of disease or injury) is a major concern in the United States. Opioids are the most commonly prescribed medication to treat patients with chronic non-malignant pain. However, in one systematic review of chronic low back pain, the authors note that, although clinical trials suggest that opioids are effective for short-term use (≤ 16 weeks), the effectiveness of long-term opioids (\> 16 weeks) for pain relief and improved physical functioning is less clear. Five to 31 percent of chronic back pain patients prescribed long-term opioids show aberrant drug-taking behaviors. Many develop tolerance and withdrawal, 43% of these patients exhibit opioid addiction. Therefore, patients with chronic pain and a co-occurring opioid addiction present a clinical challenge. In such cases, referral to addiction experts is recommended, but specialized treatment is currently based on expert opinion and observational studies. The expert recommendation is detoxification followed by treatment with methadone, buprenorphine, naltrexone, or non-opioid analgesics in conjunction with behavioral counseling. Discontinuing short-acting opioid medications increases pain and will make it difficult for these patients to abstain from opioids due to the severity of pain. However, continuing these opioid medications worsens their addiction and renders opioids ineffective in the treatment of pain. Research is needed to compare the various medication-assisted treatments. Long-acting opioids (e.g., methadone, buprenorphine) are used to replace treatment with short-acting opioids (e.g., hydrocodone, oxycodone). Methadone is a full mu-opioid-receptor agonist that can be effective in treating pain. Two small studies suggest that treatment of patients with chronic pain and co-occurring substance use disorder with methadone and adjunctive pain management therapy is superior to non-opioid treatment protocols. Despite the demonstration that methadone can be effective as both an analgesic and for opioid addiction treatment, it possesses side effects (e.g, constipation) and serious adverse events (e.g, respiratory depression, risk of overdose) that limit its use, making physicians reluctant to prescribe methadone. Buprenorphine, a partial opioid agonist, is an alternative to methadone for treatment of opioid addiction, has a safety profile superior to methadone, and possesses analgesic properties. For outpatient use, buprenorphine is combined with naloxone (BUP/NLX) to reduce the potential for abuse (i.e., IV administration). When given to those who abuse prescription opioids BUP/NLX possesses better treatment outcomes than those who abuse heroin. In one uncontrolled case series of 95 participants, Malinoff and his colleagues concluded that the effectiveness in the treatment of opioid dependence, in providing analgesia, and the low abuse liability make BUP/NLX a potentially useful treatment for patients with chronic pain and co-occurring opioid addiction. In a randomized controlled trial by Blondell et al. (2010), treatment with BUP/NLX was superior to the abstinence-oriented approach in regards to treatment retention in patients with chronic pain and co-existent opioid addiction. However, there has not been a randomized clinical trial comparing BUP/NLX with methadone maintenance in chronic pain patients with opioid addiction. Preliminary data suggest that both 6-months BUP/NLX and methadone treatment results analgesia, but methadone treatment results in better addiction outcomes. The present study is designed to determine the complexity of recovery outcomes (e.g., functioning, mental health) in chronic pain patients. Clinicians need evidence-based guidelines to more effectively manage patients who have both chronic pain and evidence of opioid misuse or addiction behaviors. In this study, we plan to investigate whether patients treated with BUP/NLX and usual care will have improved clinical outcomes as those provided with methadone treatment and usual care. Specifically, we propose to give 63 patients BUP/NLX therapy for 6 months (experimental group) and 63 patients methadone therapy over 6 (active comparator). We hypothesize that patients given BUP/NLX treatment will have similar outcomes as those receiving methadone maintenance with respect to functioning, mental health, pain level, and treatment retention.

Interventions

DRUGMethadone

10-60 mg/day divided by 2-4 times a day for 6 months

DRUGBuprenorphine/naloxone

4-16 mg/day divided by 2-4 times a day for 6 months

Sponsors

State University of New York at Buffalo
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

1. have a well-documented chronic pain disorder due to past back surgery, 2. have a chronic back pain syndrome, 3. have evidence of opioid addiction, 4. prior attempt at abstinence-oriented treatment documented by the referring physician, 5. be able to understand spoken and written English, 6. reside in Erie or Niagara counties, 7. have health insurance or other ability to pay for treatment with the approval from patient's primary physician; 8. have no prior history of methadone or BUP/NLX maintenance treatment since the last surgery, 9. not be a member of a vulnerable population, including prisoners

Exclusion criteria

1. homeless, or any patient without a locator (no means to participate in the follow-up data collection interviews by phone), 2. inability to give consent, 3. those with major co-occurring psychiatric disorders, 4. EKG showing prolonged QT and/or previous cardiac issues, 5. are taking a medication that is contraindicated with methadone, 6. medically unstable, 7. urine positive for cocaine at initial visit, 8. pregnant women

Design outcomes

Primary

MeasureTime frameDescription
Analgesia6 monthsPain severity will be measured using the Visual Analogue Scale (VAS) which has a range of 0-100 with 0 being no pain and 100 being worse possible pain.

Secondary

MeasureTime frameDescription
Illicit Drug Use6 monthsIllicit opioid use will be measured by self-report and confirmed with urine toxicology.
Cravingsat 6 monthsCravings will be assessed using the Visual Analogue Scale (VAS) with 0 being no cravings and 100 being worse possible cravings
Functioningat 6 monthsFunctioning will be assessed using the Visual Analogue Scale (VAS) with 0 being no limits and 100 being bedridden.
Depressionat 6 monthsDepression will be assessed using the Beck Depression Inventory, a 63 point scale with 0 being none and 63 being severe.
Treatment Retention6 monthsNumber of participants that completed the study protocol

Countries

United States

Participant flow

Recruitment details

Recruitment occurred between January 2012 and December 2013 at an ambulatory care medical clinic. Follow-up data collection lasted until May 2014

Pre-assignment details

25 participants were assessed, but 6 were excluded for: unwilling to be randomized, DAST score below minimum, not opioid dependent, prior maintenance therapy, no prior surgery, and initial toxicology positive for cocaine (one patient per category)

Participants by arm

ArmCount
Methadone
10-60 mg/day divided by 2-4 times a day Methadone: 10-60 mg/day divided by 2-4 times a day for 6 months
9
Buprenorphine/Naloxone
4-16 mg/day divided by 2-4 times a day Buprenorphine/naloxone: 4-16 mg/day divided by 2-4 times a day for 6 months
10
Total19

Withdrawals & dropouts

PeriodReasonFG000FG001
Overall StudyLack of Efficacy01
Overall StudyLost to Follow-up32
Overall StudyPhysician Decision01
Overall StudyProtocol Violation01
Overall StudyWithdrawal by Subject01

Baseline characteristics

CharacteristicMethadoneBuprenorphine/NaloxoneTotal
Age, Categorical
<=18 years
0 Participants0 Participants0 Participants
Age, Categorical
>=65 years
0 Participants0 Participants0 Participants
Age, Categorical
Between 18 and 65 years
9 Participants10 Participants19 Participants
Age, Continuous44.44 years
STANDARD_DEVIATION 11.85
38.20 years
STANDARD_DEVIATION 9.16
41.16 years
STANDARD_DEVIATION 10.71
criminal history
any prior arrest
4 participants1 participants5 participants
criminal history
no prior arrests
5 participants9 participants14 participants
current treatment for back pain
current treatment
6 participants6 participants12 participants
current treatment for back pain
past treatment
3 participants4 participants7 participants
disabled
disabled
7 participants6 participants13 participants
disabled
not disabled
2 participants4 participants6 participants
drug and alcohol treatment history
no past addiction treatment
7 participants7 participants14 participants
drug and alcohol treatment history
past addiction treatment
2 participants3 participants5 participants
education
high school or less
6 participants4 participants10 participants
education
some college
3 participants6 participants9 participants
Ethnicity (NIH/OMB)
Hispanic or Latino
0 Participants0 Participants0 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
9 Participants10 Participants19 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants
never married
current of prior marriage
6 participants4 participants10 participants
never married
never married
3 participants6 participants9 participants
past lower back surgery
other spinal surgery
6 participants4 participants10 participants
past lower back surgery
past lower back surgery
3 participants6 participants9 participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Asian
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Black or African American
1 Participants2 Participants3 Participants
Race (NIH/OMB)
More than one race
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Unknown or Not Reported
1 Participants0 Participants1 Participants
Race (NIH/OMB)
White
7 Participants8 Participants15 Participants
Region of Enrollment
United States
9 participants10 participants19 participants
Sex: Female, Male
Female
7 Participants6 Participants13 Participants
Sex: Female, Male
Male
2 Participants4 Participants6 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
— / —— / —
other
Total, other adverse events
0 / 90 / 10
serious
Total, serious adverse events
1 / 90 / 10

Outcome results

Primary

Analgesia

Pain severity will be measured using the Visual Analogue Scale (VAS) which has a range of 0-100 with 0 being no pain and 100 being worse possible pain.

Time frame: 6 months

Population: 19 participants were enrolled in the study, and 10 were available for the 6-month follow-up.

ArmMeasureValue (MEAN)Dispersion
MethadoneAnalgesia36.3 units on a VAS scaleStandard Deviation 22.4
Buprenorphine/NaloxoneAnalgesia71.8 units on a VAS scaleStandard Deviation 20.9
p-value: 0.09795% CI: [-8.7519, 79.5852]t-test, 2 sided
Secondary

Cravings

Cravings will be assessed using the Visual Analogue Scale (VAS) with 0 being no cravings and 100 being worse possible cravings

Time frame: at 6 months

ArmMeasureValue (MEAN)Dispersion
MethadoneCravings11.7 units on a VAS scaleStandard Deviation 18.1
Buprenorphine/NaloxoneCravings27.2 units on a VAS scaleStandard Deviation 31.7
p-value: 0.34895% CI: [-20.37051, 51.34968]t-test, 2 sided
Secondary

Depression

Depression will be assessed using the Beck Depression Inventory, a 63 point scale with 0 being none and 63 being severe.

Time frame: at 6 months

ArmMeasureValue (MEAN)Dispersion
MethadoneDepression17.0 units on a BDI scaleStandard Deviation 18.2
Buprenorphine/NaloxoneDepression15.3 units on a BDI scaleStandard Deviation 14.2
p-value: 0.89595% CI: [-30.3965, 27.0632]t-test, 2 sided
Secondary

Functioning

Functioning will be assessed using the Visual Analogue Scale (VAS) with 0 being no limits and 100 being bedridden.

Time frame: at 6 months

ArmMeasureValue (MEAN)Dispersion
MethadoneFunctioning31.7 units on a VAS scaleStandard Deviation 25.1
Buprenorphine/NaloxoneFunctioning71.3 units on a VAS scaleStandard Deviation 16
p-value: 0.08895% CI: [-7.9653, 87.132]t-test, 2 sided
Secondary

Illicit Drug Use

Illicit opioid use will be measured by self-report and confirmed with urine toxicology.

Time frame: 6 months

Population: 19 participants were enrolled in the study, and 10 were available at the 6-month follow-up

ArmMeasureGroupValue (NUMBER)
MethadoneIllicit Drug Useillicit drug use at 6 months0 participants
MethadoneIllicit Drug Useno illicit drug use at 6 months6 participants
Buprenorphine/NaloxoneIllicit Drug Useillicit drug use at 6 months0 participants
Buprenorphine/NaloxoneIllicit Drug Useno illicit drug use at 6 months4 participants
p-value: 195% CI: [0.0713, 1.8248]Fisher Exact
Secondary

Treatment Retention

Number of participants that completed the study protocol

Time frame: 6 months

ArmMeasureGroupValue (NUMBER)
MethadoneTreatment Retentiondid not complete3 participants
MethadoneTreatment Retentioncompleted6 participants
Buprenorphine/NaloxoneTreatment Retentiondid not complete6 participants
Buprenorphine/NaloxoneTreatment Retentioncompleted4 participants
p-value: 0.699995% CI: [0.127, 2.8352]Fisher Exact

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