Completed

Phase 3
Age: 21Years - 50Years
All Genders
ID00000205

Buprenorphine Maintenance Protocol

Led by University of California, Los Angeles · Updated on 2016-07-11

N/A

Participants Needed

1

Research Sites

26 weeks

Total Duration

On this page

Sponsors

U

University of California, Los Angeles

Lead Sponsor

N

National Institute on Drug Abuse (NIDA)

Collaborating Sponsor

AI-Summary

What this Trial Is About

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

CONDITIONS

Official Title

Buprenorphine Maintenance Protocol - 1

Who Can Participate

Age: 21Years - 50Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

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.

Not Eligible

You will not qualify if you...

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

Trial Site Locations

Total: 1 location

1

Friends Research Institute

Los Angeles, California, United States, 90025

Status Unknown

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

N/A

Model

N/A

Primary Purpose

TREATMENT

Number of Arms

0

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Published Research Related To This Trial