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Buprenorphine Maintenance Protocol - 1

This study has been completed.

Sponsored by: National Institute on Drug Abuse (NIDA)
Information provided by: National Institute on Drug Abuse (NIDA)
ClinicalTrials.gov Identifier: NCT00000205
  Purpose

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


Condition Intervention Phase
Opioid-Related Disorders
Drug: Buprenorphine
Phase III

ChemIDplus related topics:   Buprenorphine    Buprenorphine hydrochloride   

U.S. FDA Resources

Study Type:   Interventional
Study Design:   Treatment, Double-Blind, Placebo Control
Official Title:   Buprenorphine Maintenance Protocol

Further study details as provided by National Institute on Drug Abuse (NIDA):

Primary Outcome Measures:
  • Retention
  • Opiate use
  • Opiate craving
  • Adverse events

Estimated Enrollment:   0
Study Start Date:   October 1990

  Eligibility
Ages Eligible for Study:   21 Years to 50 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No

Criteria

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

  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00000205

Locations
United States, California
Friends Research Institute    
      Los Angeles, California, United States, 90025

Sponsors and Collaborators

Investigators
Principal Investigator:     Walter Ling, M.D.     Friends Research Institute, Inc.    
  More Information


Study ID Numbers:   NIDA-06082-1, R18-06082-1
First Received:   September 20, 1999
Last Updated:   November 3, 2005
ClinicalTrials.gov Identifier:   NCT00000205
Health Authority:   United States: Federal Government

Study placed in the following topic categories:
Buprenorphine
Mental Disorders
Substance-Related Disorders
Disorders of Environmental Origin
Opioid-Related Disorders

Additional relevant MeSH terms:
Sensory System Agents
Therapeutic Uses
Narcotic Antagonists
Physiological Effects of Drugs
Central Nervous System Depressants
Narcotics
Peripheral Nervous System Agents
Analgesics
Central Nervous System Agents
Pharmacologic Actions
Analgesics, Opioid

ClinicalTrials.gov processed this record on October 07, 2008




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