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NCT00000235 Clinical Trial

Alternate Day Buprenorphine Administration, Phase XII - 17

Opioid-Related Disorders Clinical Trial

Official title:
Alternate Day Buprenorphine Administration, Phase XII

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00000235
Other study ID # NIDA-06969-17
Secondary ID R01-06969-17
Status Completed
Phase Phase 2
First received September 20, 1999
Last updated August 16, 2005

Study information
Verified date December 2002
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 determine if six times daily buprenorphine dose is effective in achieving 120 hour buprenorphine dosing.

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

Study Design

Intervention Model: Crossover Assignment, 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 Opioid withdrawal
Primary Opioid agonist effects
Primary Dose choice
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