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Alternate-Day Buprenorphine Administration. Phase VI - 7

This study has been completed.
Study NCT00000225.   Last updated on June 23, 2005.   Information provided by National Institute on Drug Abuse (NIDA)

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Descriptive Information Fields
Brief Title  Alternate-Day Buprenorphine Administration. Phase VI - 7
Official Title  Alternate-Day Buprenorphine Administration. Phase VI
Brief Summary

The purpose of this study is to determine if four times a subject's daily maintenance dose will hold for 96 hours without changes in agonist and antagonist effects.

Detailed Description
Study Phase Phase II
Study Type  Interventional
Study Design  Treatment, Double-Blind, Placebo Control
Primary Outcome Measure  Drug use
Opioid withdrawal
Opioid agonist effects
Dose identification
Pupil diameter
Secondary Outcome Measure 
Condition  Opioid-Related Disorders
Intervention  Drug: Buprenorphine
MEDLINE PMIDs
Links
Recruitment Information Fields
Recruitment Status  Completed
Enrollment  0
Start Date  December 1992
Completion Date
Eligibility Criteria 

Please contact site for information.

Gender Both
Ages 21 Years to 51 Years
Accepts Healthy Volunteers No
Contacts ††
Location Countries  United States
Administrative Information Fields
NCT ID  NCT00000225
Organization ID NIDA-06969-7
Secondary IDs †† R01-06969-7
Study Sponsor  National Institute on Drug Abuse (NIDA)
Collaborators †† University of Vermont
Investigators 
Principal Investigator:     Warren Bickel, Ph.D.     University of Vermont    
Information Provided By National Institute on Drug Abuse (NIDA)
Verification Date June 2004
First Received Date  September 20, 1999
Last Updated Date June 23, 2005

 †    Required WHO trial registration data element.
††   WHO trial registration data element that is required only if it exists.




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