Low Back Pain
Conditions
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
10-60 mg/day divided by 2-4 times a day for 6 months
4-16 mg/day divided by 2-4 times a day for 6 months
Sponsors
Study design
Eligibility
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
| Measure | Time frame | Description |
|---|---|---|
| Analgesia | 6 months | 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. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Illicit Drug Use | 6 months | Illicit opioid use will be measured by self-report and confirmed with urine toxicology. |
| Cravings | at 6 months | Cravings will be assessed using the Visual Analogue Scale (VAS) with 0 being no cravings and 100 being worse possible cravings |
| Functioning | at 6 months | Functioning will be assessed using the Visual Analogue Scale (VAS) with 0 being no limits and 100 being bedridden. |
| Depression | at 6 months | Depression will be assessed using the Beck Depression Inventory, a 63 point scale with 0 being none and 63 being severe. |
| Treatment Retention | 6 months | Number 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
| Arm | Count |
|---|---|
| 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 |
| Total | 19 |
Withdrawals & dropouts
| Period | Reason | FG000 | FG001 |
|---|---|---|---|
| Overall Study | Lack of Efficacy | 0 | 1 |
| Overall Study | Lost to Follow-up | 3 | 2 |
| Overall Study | Physician Decision | 0 | 1 |
| Overall Study | Protocol Violation | 0 | 1 |
| Overall Study | Withdrawal by Subject | 0 | 1 |
Baseline characteristics
| Characteristic | Methadone | Buprenorphine/Naloxone | Total |
|---|---|---|---|
| Age, Categorical <=18 years | 0 Participants | 0 Participants | 0 Participants |
| Age, Categorical >=65 years | 0 Participants | 0 Participants | 0 Participants |
| Age, Categorical Between 18 and 65 years | 9 Participants | 10 Participants | 19 Participants |
| Age, Continuous | 44.44 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 participants | 1 participants | 5 participants |
| criminal history no prior arrests | 5 participants | 9 participants | 14 participants |
| current treatment for back pain current treatment | 6 participants | 6 participants | 12 participants |
| current treatment for back pain past treatment | 3 participants | 4 participants | 7 participants |
| disabled disabled | 7 participants | 6 participants | 13 participants |
| disabled not disabled | 2 participants | 4 participants | 6 participants |
| drug and alcohol treatment history no past addiction treatment | 7 participants | 7 participants | 14 participants |
| drug and alcohol treatment history past addiction treatment | 2 participants | 3 participants | 5 participants |
| education high school or less | 6 participants | 4 participants | 10 participants |
| education some college | 3 participants | 6 participants | 9 participants |
| Ethnicity (NIH/OMB) Hispanic or Latino | 0 Participants | 0 Participants | 0 Participants |
| Ethnicity (NIH/OMB) Not Hispanic or Latino | 9 Participants | 10 Participants | 19 Participants |
| Ethnicity (NIH/OMB) Unknown or Not Reported | 0 Participants | 0 Participants | 0 Participants |
| never married current of prior marriage | 6 participants | 4 participants | 10 participants |
| never married never married | 3 participants | 6 participants | 9 participants |
| past lower back surgery other spinal surgery | 6 participants | 4 participants | 10 participants |
| past lower back surgery past lower back surgery | 3 participants | 6 participants | 9 participants |
| Race (NIH/OMB) American Indian or Alaska Native | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Asian | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Black or African American | 1 Participants | 2 Participants | 3 Participants |
| Race (NIH/OMB) More than one race | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Native Hawaiian or Other Pacific Islander | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Unknown or Not Reported | 1 Participants | 0 Participants | 1 Participants |
| Race (NIH/OMB) White | 7 Participants | 8 Participants | 15 Participants |
| Region of Enrollment United States | 9 participants | 10 participants | 19 participants |
| Sex: Female, Male Female | 7 Participants | 6 Participants | 13 Participants |
| Sex: Female, Male Male | 2 Participants | 4 Participants | 6 Participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk |
|---|---|---|
| deaths Total, all-cause mortality | — / — | — / — |
| other Total, other adverse events | 0 / 9 | 0 / 10 |
| serious Total, serious adverse events | 1 / 9 | 0 / 10 |
Outcome results
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.
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Methadone | Analgesia | 36.3 units on a VAS scale | Standard Deviation 22.4 |
| Buprenorphine/Naloxone | Analgesia | 71.8 units on a VAS scale | Standard Deviation 20.9 |
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
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Methadone | Cravings | 11.7 units on a VAS scale | Standard Deviation 18.1 |
| Buprenorphine/Naloxone | Cravings | 27.2 units on a VAS scale | Standard Deviation 31.7 |
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
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Methadone | Depression | 17.0 units on a BDI scale | Standard Deviation 18.2 |
| Buprenorphine/Naloxone | Depression | 15.3 units on a BDI scale | Standard Deviation 14.2 |
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
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Methadone | Functioning | 31.7 units on a VAS scale | Standard Deviation 25.1 |
| Buprenorphine/Naloxone | Functioning | 71.3 units on a VAS scale | Standard Deviation 16 |
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
| Arm | Measure | Group | Value (NUMBER) |
|---|---|---|---|
| Methadone | Illicit Drug Use | illicit drug use at 6 months | 0 participants |
| Methadone | Illicit Drug Use | no illicit drug use at 6 months | 6 participants |
| Buprenorphine/Naloxone | Illicit Drug Use | illicit drug use at 6 months | 0 participants |
| Buprenorphine/Naloxone | Illicit Drug Use | no illicit drug use at 6 months | 4 participants |
Treatment Retention
Number of participants that completed the study protocol
Time frame: 6 months
| Arm | Measure | Group | Value (NUMBER) |
|---|---|---|---|
| Methadone | Treatment Retention | did not complete | 3 participants |
| Methadone | Treatment Retention | completed | 6 participants |
| Buprenorphine/Naloxone | Treatment Retention | did not complete | 6 participants |
| Buprenorphine/Naloxone | Treatment Retention | completed | 4 participants |