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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.
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.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Methadone | Active Comparator | 10-60 mg/day divided by 2-4 times a day |
|
| Buprenorphine/naloxone | Experimental | 4-16 mg/day divided by 2-4 times a day |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Methadone | Drug | 10-60 mg/day divided by 2-4 times a day for 6 months |
|
| Measure | Description | Time Frame |
|---|---|---|
| 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. | 6 months |
| Measure | Description | Time Frame |
|---|---|---|
| Illicit Drug Use | Illicit opioid use will be measured by self-report and confirmed with urine toxicology. | 6 months |
| Cravings | Cravings will be assessed using the Visual Analogue Scale (VAS) with 0 being no cravings and 100 being worse possible cravings |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Rachel A Rizzo, MPH | University at Buffalo | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| UB/MD Family Medicine, Inc. | Amherst | New York | 14228 | United States |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 23480249 | Background | Neumann AM, Blondell RD, Jaanimagi U, Giambrone AK, Homish GG, Lozano JR, Kowalik U, Azadfard M. A preliminary study comparing methadone and buprenorphine in patients with chronic pain and coexistent opioid addiction. J Addict Dis. 2013;32(1):68-78. doi: 10.1080/10550887.2012.759872. | |
| 36063082 | Derived | Nielsen S, Tse WC, Larance B. Opioid agonist treatment for people who are dependent on pharmaceutical opioids. Cochrane Database Syst Rev. 2022 Sep 5;9(9):CD011117. doi: 10.1002/14651858.CD011117.pub3. |
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We are preparing a de-identified data set that could be shared.
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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)
Recruitment occurred between January 2012 and December 2013 at an ambulatory care medical clinic. Follow-up data collection lasted until May 2014
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| ID | Title | Description |
|---|---|---|
| FG000 | 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 |
| FG001 | 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 |
| Title | Milestones | Reasons Not Completed | |||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
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|
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| ID | Title | Description |
|---|---|---|
| BG000 | 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 |
| BG001 | 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 |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Categorical | Count of Participants |
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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. | 19 participants were enrolled in the study, and 10 were available for the 6-month follow-up. | Posted | Mean | Standard Deviation | units on a VAS scale | 6 months |
|
6 months
Drug overdose
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Methadone | Methadone 10-60 mg/day divided 2-4 times a day for 6 months |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| drug overdose | Social circumstances | Non-systematic Assessment |
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Early termination due to human subject concerns
| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Dr. Ricahrd Blondell | University at Buffalo | 716-816-7237 | blondell@buffalo.edu |
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| ID | Term |
|---|---|
| D017116 | Low Back Pain |
| D059350 | Chronic Pain |
| D009293 | Opioid-Related Disorders |
| D019966 | Substance-Related Disorders |
| ID | Term |
|---|---|
| D001416 | Back Pain |
| D010146 | Pain |
| D009461 | Neurologic Manifestations |
| D012816 | Signs and Symptoms |
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| ID | Term |
|---|---|
| D008691 | Methadone |
| D000069479 | Buprenorphine, Naloxone Drug Combination |
| ID | Term |
|---|---|
| D007659 | Ketones |
| D009930 | Organic Chemicals |
| D002047 | Buprenorphine |
| D009019 | Morphinans |
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| Buprenorphine/naloxone | Drug | 4-16 mg/day divided by 2-4 times a day for 6 months |
|
|
| at 6 months |
| Functioning | Functioning will be assessed using the Visual Analogue Scale (VAS) with 0 being "no limits" and 100 being "bedridden." | at 6 months |
| Depression | Depression will be assessed using the Beck Depression Inventory, a 63 point scale with 0 being "none" and 63 being "severe." | at 6 months |
| Treatment Retention | Number of participants that completed the study protocol | 6 months |
| 31774028 | Derived | Neumann AM, Blondell RD, Hoopsick RA, Homish GG. Randomized clinical trial comparing buprenorphine/naloxone and methadone for the treatment of patients with failed back surgery syndrome and opioid addiction. J Addict Dis. 2020 Jan-Mar;38(1):33-41. doi: 10.1080/10550887.2019.1690929. Epub 2019 Nov 27. |
| Physician Decision |
|
| Protocol Violation |
|
| Lack of Efficacy |
|
| BG002 | Total | Total of all reporting groups |
| Participants |
|
| Age, Continuous | Mean | Standard Deviation | years |
|
| Sex: Female, Male | Count of Participants | Participants |
|
| Ethnicity (NIH/OMB) | Count of Participants | Participants |
|
| Race (NIH/OMB) | Count of Participants | Participants |
|
| Region of Enrollment | Number | participants |
|
| disabled | Number | participants |
|
| never married | Number | participants |
|
| past lower back surgery | Number | participants |
|
| current treatment for back pain | Number | participants |
|
| drug and alcohol treatment history | Number | participants |
|
| criminal history | Number | participants |
|
| education | Number | participants |
|
|
|
|
| Secondary | Illicit Drug Use | Illicit opioid use will be measured by self-report and confirmed with urine toxicology. | 19 participants were enrolled in the study, and 10 were available at the 6-month follow-up | Posted | Number | participants | 6 months |
|
|
|
|
| Secondary | Cravings | Cravings will be assessed using the Visual Analogue Scale (VAS) with 0 being no cravings and 100 being worse possible cravings | Posted | Mean | Standard Deviation | units on a VAS scale | at 6 months |
|
|
|
|
| Secondary | Functioning | Functioning will be assessed using the Visual Analogue Scale (VAS) with 0 being "no limits" and 100 being "bedridden." | Posted | Mean | Standard Deviation | units on a VAS scale | at 6 months |
|
|
|
|
| Secondary | Depression | Depression will be assessed using the Beck Depression Inventory, a 63 point scale with 0 being "none" and 63 being "severe." | Posted | Mean | Standard Deviation | units on a BDI scale | at 6 months |
|
|
|
|
| Secondary | Treatment Retention | Number of participants that completed the study protocol | Posted | Number | participants | 6 months |
|
|
|
|
| 1 |
| 9 |
| 0 |
| 9 |
| EG001 | Buprenorphine/Naloxone | Buprenorphine 4-16 mg/day divided 2-4 times a day for 6 months | 0 | 10 | 0 | 10 |
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| D013568 |
| Pathological Conditions, Signs and Symptoms |
| D000079524 | Narcotic-Related Disorders |
| D064419 | Chemically-Induced Disorders |
| D001523 | Mental Disorders |
| D053610 |
| Opiate Alkaloids |
| D000470 | Alkaloids |
| D006571 | Heterocyclic Compounds |
| D009270 | Naloxone |
| D006572 | Heterocyclic Compounds, Bridged-Ring |
| D006576 | Heterocyclic Compounds, 4 or More Rings |
| D000072471 | Heterocyclic Compounds, Fused-Ring |
| D010616 | Phenanthrenes |
| D011084 | Polycyclic Aromatic Hydrocarbons |
| D011083 | Polycyclic Compounds |
| D004338 | Drug Combinations |
| D004364 | Pharmaceutical Preparations |