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Buprenorphine and Methadone for Opioid-dependent Chronic Back Pain Patients

Primary Purpose

Low Back Pain

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Methadone
Buprenorphine/naloxone
Sponsored by
State University of New York at Buffalo
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Low Back Pain focused on measuring chronic pain, opioid dependence, methadone, buprenorphine, substance use disorder

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • UB/MD Family Medicine, Inc.

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Methadone

Buprenorphine/naloxone

Arm Description

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

4-16 mg/day divided by 2-4 times a day

Outcomes

Primary Outcome Measures

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.

Secondary Outcome Measures

Illicit Drug Use
Illicit opioid use will be measured by self-report and confirmed with urine toxicology.
Cravings
Cravings will be assessed using the Visual Analogue Scale (VAS) with 0 being no cravings and 100 being worse possible cravings
Functioning
Functioning will be assessed using the Visual Analogue Scale (VAS) with 0 being "no limits" and 100 being "bedridden."
Depression
Depression will be assessed using the Beck Depression Inventory, a 63 point scale with 0 being "none" and 63 being "severe."
Treatment Retention
Number of participants that completed the study protocol

Full Information

First Posted
March 19, 2012
Last Updated
October 12, 2020
Sponsor
State University of New York at Buffalo
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1. Study Identification

Unique Protocol Identification Number
NCT01559454
Brief Title
Buprenorphine and Methadone for Opioid-dependent Chronic Back Pain Patients
Official Title
A Randomized Controlled Trial Comparing Buprenorphine and Methadone for Treatment in Opioid Dependent Chronic Back Pain Patients
Study Type
Interventional

2. Study Status

Record Verification Date
October 2020
Overall Recruitment Status
Completed
Study Start Date
February 2012 (undefined)
Primary Completion Date
May 2014 (Actual)
Study Completion Date
May 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
State University of New York at Buffalo

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Low Back Pain
Keywords
chronic pain, opioid dependence, methadone, buprenorphine, substance use disorder

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
19 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Methadone
Arm Type
Active Comparator
Arm Description
10-60 mg/day divided by 2-4 times a day
Arm Title
Buprenorphine/naloxone
Arm Type
Experimental
Arm Description
4-16 mg/day divided by 2-4 times a day
Intervention Type
Drug
Intervention Name(s)
Methadone
Other Intervention Name(s)
Dolophine
Intervention Description
10-60 mg/day divided by 2-4 times a day for 6 months
Intervention Type
Drug
Intervention Name(s)
Buprenorphine/naloxone
Other Intervention Name(s)
Suboxone
Intervention Description
4-16 mg/day divided by 2-4 times a day for 6 months
Primary Outcome Measure Information:
Title
Analgesia
Description
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
Secondary Outcome Measure Information:
Title
Illicit Drug Use
Description
Illicit opioid use will be measured by self-report and confirmed with urine toxicology.
Time Frame
6 months
Title
Cravings
Description
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
Title
Functioning
Description
Functioning will be assessed using the Visual Analogue Scale (VAS) with 0 being "no limits" and 100 being "bedridden."
Time Frame
at 6 months
Title
Depression
Description
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
Title
Treatment Retention
Description
Number of participants that completed the study protocol
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: have a well-documented chronic pain disorder due to past back surgery, have a chronic back pain syndrome, have evidence of opioid addiction, prior attempt at abstinence-oriented treatment documented by the referring physician, be able to understand spoken and written English, reside in Erie or Niagara counties, have health insurance or other ability to pay for treatment with the approval from patient's primary physician; have no prior history of methadone or BUP/NLX maintenance treatment since the last surgery, not be a member of a vulnerable population, including prisoners Exclusion Criteria: homeless, or any patient without a "locator" (no means to participate in the follow-up data collection interviews by phone), inability to give consent, those with major co-occurring psychiatric disorders, EKG showing prolonged QT and/or previous cardiac issues, are taking a medication that is contraindicated with methadone, medically unstable, urine positive for cocaine at initial visit, pregnant women
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rachel A Rizzo, MPH
Organizational Affiliation
University at Buffalo
Official's Role
Study Director
Facility Information:
Facility Name
UB/MD Family Medicine, Inc.
City
Amherst
State/Province
New York
ZIP/Postal Code
14228
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Undecided
IPD Sharing Plan Description
We are preparing a de-identified data set that could be shared.
Citations:
PubMed Identifier
23480249
Citation
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.
Results Reference
background
PubMed Identifier
36063082
Citation
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.
Results Reference
derived
PubMed Identifier
31774028
Citation
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.
Results Reference
derived

Learn more about this trial

Buprenorphine and Methadone for Opioid-dependent Chronic Back Pain Patients

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