Buprenorphine Maintenance Treatment of Opioid Dependence in Primary Care: A Randomized Clinical Trial

Phase 2

Completed

• Conditions: Opioid-Related Disorders; Heroin Dependence
• Interventions: Drug: Buprenorphine

• Registration Number: NCT00684554
• Lead Sponsor: New York State Psychiatric Institute

Brief Summary

The study will assess the effectiveness of at-home vs. in-office induction for patients entering buprenorphine maintenance at Associates in Internal Medicine (AIM) primary care clinic.

Detailed Description

Buprenorphine maintenance is an effective treatment for opioid dependence, yet diffusion has been limited. Physician concern about induction is a reported barrier, primarily as buprenorphine may precipitate withdrawal due to its partial opioid agonist activity and high receptor binding affinity. To minimize risk, guidelines recommend in-office assessment and monitoring during induction. As this may not be feasible (e.g., time limitations), many patients are instructed to self-induct at home. While this may facilitate treatment entry, data on at-home induction are limited. The study will assess the effectiveness of at-home vs. in-office induction for patients entering buprenorphine maintenance at Associates in Internal Medicine (AIM) primary care clinic. Currently, patients receive buprenorphine maintenance at AIM as part of standard clinical practice and through an observational study (IRB 5258). Most patients are insured through Medicaid, which covers visit, medication (obtained through prescription from a local pharmacy), lab, and outside psychosocial treatment cost. In this demonstration project, 20 opioid dependent patients will be randomly assigned to at-home or in-office induction, and then monitored for 12 weeks. Ancillary psychosocial treatment will be encouraged but not required. After randomization, AIM clinic and NYSPI research visits will be scheduled weekly for 4 weeks, and then at weeks 8 and 12. The primary outcome will include a comparison of the proportion of patients successfully inducted one week after the initial primary care visit. Secondary outcomes will include: 1) Time to stabilization after buprenorphine initiation assessed by: a) Time until the patient is without withdrawal for two consecutive days, and b) Time until the patient is opioid free for two consecutive weeks; and 3) Retention-in-treatment at 4 and 12 weeks. Other secondary outcomes include patient satisfaction and change in addiction severity. These data will provide important information in buprenorphine initiation in primary care and enable determination of treatment effects size prior to future clinical trials.

Study Timeline

• Study Start: 2007-12
• Study First Submitted: 2008-05-22
• Study First Submitted QC: 2008-05-22
• Study First Posted: 2008-05-26
• Primary Completion: 2008-08
• Study Completion: 2010-04
• Results First Submitted: 2015-05-19
• Results First Submitted QC: 2015-12-07
• Results First Posted: 2016-01-11
• Status Verified: 2019-04
• Last Update Submitted: 2019-04-22
• Last Update Posted: 2019-04-24

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 20

Inclusion Criteria

1. DSM-IV criteria for current opioid dependence with physical dependence and are seeking treatment
2. Recent opioid use
3. Individuals must describe opioids as their primary drug of abuse.
4. 18-65 years of age
5. Able to give informed consent and comply with study procedures
6. Financially able to receive treatment at AIM and obtain medication (e.g., Medicaid)

Exclusion Criteria

1. DSM-IV opioid dependence without physical dependence
2. Any current Axis I psychiatric disorder(s) as defined by DSM-IV-TR that in the investigator's judgment are unstable or would be disrupted by study participation (e.g., psychosis, active suicidal or homicidal ideation).
3. Individuals who are significant risk for suicide based on their current mental state or history.
4. DSM-IV alcohol or benzodiazepine dependence with physiologic dependence.
5. Pregnancy, lactation. Women must also agree to use a method of contraception with proven efficacy and agree not to become pregnant during the study.
6. Unstable physical disorder that might make participation hazardous.
7. Individuals with a known allergy, sensitivity or adverse reaction to buprenorphine.
8. Past life-threatening idiosyncratic severe opioid withdrawal reaction (e.g., psychosis, seizure)
9. Current buprenorphine maintenance
10. Current long-acting opioid use (e.g., methadone)
11. Inability to read or understand the self-report assessment forms unaided

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Unobserved-at home	Buprenorphine	Buprenorphine Unobserved at home induction
Observed	Buprenorphine	Buprenorphine Observed in office induction

Primary Outcome Measures

Name	Time	Method
The Primary Outcome Will Include a Comparison of the Proportion of Patients Successfully Inducted One Week After the Initial Primary Care Visit.	one week after initial primary care visit	The primary outcome will include a comparison of the proportion of patients successfully inducted one week after the initial primary care visit. Defined as in treatment, on Buprenorphine and withdrawal free.

Secondary Outcome Measures

Name	Time	Method
Prolonged Withdrawal	a) 2 days	participants experiencing prolonged withdrawal beyond two days after buprenorphine induction

Trial Locations

Locations (1)

Columbia University/New York State Psychiatric Institute; 🇺🇸 New York, New York, United States