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NCT00000237 Clinical Trial

Buprenorphine Detoxification - BBDVI - 19

Opioid-Related Disorders Clinical Trial

Official title:
Buprenorphine Detoxification - BBDVI

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00000237
Other study ID # NIDA-06969-19
Secondary ID R01-06969-19
Status Completed
Phase Phase 2
First received September 20, 1999
Last updated August 16, 2005
Start date May 1997

Study information
Verified date May 1997
Source National Institute on Drug Abuse (NIDA)
Contact n/a
Is FDA regulated No
Health authority United States: Federal Government
Study type Interventional

Clinical Trial Summary

The purpose of this study is to examine the long-term efficacy of alternate-day dosing schedules in promoting treatment compliance in the absence of confounding behavioral contingencies.

Recruitment information / eligibility
Status Completed
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 65 Years
Eligibility Please contact site for information.

Study Design

Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Drug:
• Buprenorphine

Locations
Country Name City State
United States Treatment Research Center Burlington Vermont

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

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Drug use
Primary Retention
Primary Weeks abstinent
Primary Weeks continuous abstinence
Primary Overall treatment outcome
Primary Opioid dependence and psychiatric status
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