Buprenorphine Maintenance Protocol - 1

Phase 3

Completed

• Conditions: Opioid-Related Disorders

• Registration Number: NCT00000205
• Lead Sponsor: University of California, Los Angeles

Brief Summary

The purpose of this study is to compare the efficacy of buprenorphine versus methadone.

Detailed Description

Not available

Study Timeline

• Study Start: 1990-10
• Primary Completion: 1993-03
• Study Completion: 1993-09
• Study First Submitted: 1999-09-20
• Study First Submitted QC: 1999-09-20
• Study First Posted: 1999-09-21
• Status Verified: 2016-07
• Last Update Submitted: 2016-07-07
• Last Update Posted: 2016-07-11

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: Not specified

Inclusion Criteria

M/F ages 21-50. Opiate dependence according to DSM-IV criteria. Self-reported use within the last 30 days. Agreeable to conditions of study and signed informed consent.

Exclusion Criteria

Psychiatric disorder that requires medication therapy. History of seizures. Pregnant and /or nursing women. Dependence on ETOH or benzodiazepines or other sedative/hynotics. Acute hepatitis. Other medical conditions that deem participation to be unsafe

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Retention
Opiate use
Opiate craving
Adverse events

Trial Locations

Locations (1)

Friends Research Institute; 🇺🇸 Los Angeles, California, United States