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NCT00000234 Clinical Trial

Alternate Day Buprenorphine Administration, Phase XI - 16

Opioid-Related Disorders Clinical Trial

Official title:
Alternate Day Buprenorphine Administration, Phase XI

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00000234
Other study ID # NIDA-06969-16
Secondary ID R01DA006969R01-0
Status Completed
Phase Phase 2
First received September 20, 1999
Last updated May 5, 2016

Study information
Verified date December 2002
Source University of Vermont
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 evaluate open buprenorphine dosing with dose choice after open exposure.

Recruitment information / eligibility
Status Completed
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 25 Years to 51 Years
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
University of Vermont National Institute on Drug Abuse (NIDA)

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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