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NCT00000319 Clinical Trial

Buprenorphine Maintenance Dose Schedule and Treatment Setting - 2

Substance-Related Disorders Clinical Trial

Official title:
Buprenorphine Maintenance Dose Schedule and Treatment Setting

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00000319
Other study ID # NIDA-09803-2
Secondary ID R01DA009803R01-0
Status Completed
Phase Phase 2
First received
Last updated
Start date June 1996
Est. completion date January 2005

Study information
Verified date July 2020
Source Yale University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the efficacy of treating opioid-dependent individuals with buprenorphine on a thrice-weekly schedule compared to daily dosing.

Recruitment information / eligibility
Status Completed
Enrollment 0
Est. completion date January 2005
Est. primary completion date
Accepts healthy volunteers No
Gender All
Age group 21 Years to 55 Years
Eligibility Please contact site for information.

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• Buprenorphine

Locations
Country Name City State
United States APT Residential Services Division New Haven Connecticut

Sponsors (2)
Lead Sponsor Collaborator
Yale University National Institute on Drug Abuse (NIDA)

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Depression
Primary Withdrawal symptoms
Primary Opioid and cocaine use
Primary Social and psychological functioning
Primary AIDS risk behavior
Primary Opiate withdrawal symptoms
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