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NCT00078117 Clinical Trial

Suboxone: (Buprenorphine/Naloxone) Comparison of Two Taper Schedules - 1

Opioid-Related Disorders Clinical Trial

Official title:
Suboxone: (Buprenorphine/Naloxone) Comparison of Two Taper Schedules

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00078117
Other study ID # NIDA-CTN-0003-1
Secondary ID
Status Completed
Phase Phase 3
First received February 19, 2004
Last updated January 11, 2017
Start date June 2003
Est. completion date May 2005

Study information
Verified date April 2010
Source National Institute on Drug Abuse (NIDA)
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

The purpose of this protocol is to to compare the clinical utility of two dosage tapering regimens in Buprenorphine/Naloxone stabilized subjects for opiate detoxification.

Recruitment information / eligibility
Status Completed
Enrollment 516
Est. completion date May 2005
Est. primary completion date May 2005
Accepts healthy volunteers No
Gender All
Age group 15 Years to 99 Years
Eligibility Inclusion Criteria:

- Females are not pregnant or lactating

- Subjects meet DSM-IV criteria for opiate dependence, are medically and psychiatrically stable, and do not have a current history of benzodiazepine dependence abuse, dependence, or treatment

Study Design

Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Drug:
• Buprenorphine

Locations
Country Name City State
United States Addiction Research & Treatment Services (ARTS) Denver Colorado
United States Denver Health & Hospitals Authority Denver Colorado
United States Providence Behavioral Health Services Everett Washington
United States LI Jewish Health System Glen Oaks New York
United States Hartford Dispensary Hartford Connecticut
United States New York VA Medical Center New York New York
United States Norfolk CSB Norfolk Virginia
United States CODA Portland Oregon
United States South Light-Wakeview Clinic Raleigh North Carolina
United States Connecticut Counseling Centers Waterbury Connecticut
United States Coastal Horizons Center, Inc. Wilmington North Carolina

Sponsors (1)
Lead Sponsor Collaborator
University of California, Los Angeles

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Opiate abstinence
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