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Alternate Day Buprenorphine Administration, Phase X - 15

This study has been completed.
Study NCT00000233.   Last updated on August 16, 2005.   Information provided by National Institute on Drug Abuse (NIDA)

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Descriptive Information Fields
Brief Title  Alternate Day Buprenorphine Administration, Phase X - 15
Official Title  Alternate Day Buprenorphine Administration, Phase X
Brief Summary

The purpose of this study is to determine how subjects will make changes in the amount of medication received when given a monetary alternative to buprenorphine.

Detailed Description
Study Phase Phase II
Study Type  Interventional
Study Design  Treatment
Primary Outcome Measure  Opioid withdrawal
Subjective dose estimate
Drug effect characteristics: ARCI
Money choice
Secondary Outcome Measure 
Condition  Opioid-Related Disorders
Intervention  Drug: Buprenorphine
MEDLINE PMIDs
Links
Recruitment Information Fields
Recruitment Status  Completed
Enrollment  0
Start Date  May 1993
Completion Date
Eligibility Criteria 

Please contact site for information.

Gender Both
Ages 34 Years to 51 Years
Accepts Healthy Volunteers No
Contacts ††
Location Countries  United States
Administrative Information Fields
NCT ID  NCT00000233
Organization ID NIDA-06969-15
Secondary IDs †† R01-06969-15
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 September 1995
First Received Date  September 20, 1999
Last Updated Date August 16, 2005

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




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