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Alternate-Day Buprenorphine Administration. Phase VIII - 9
This study has been completed.
Study NCT00000227   Information provided by National Institute on Drug Abuse (NIDA)
First Received: September 20, 1999   Last Updated: August 16, 2005   History of Changes

September 20, 1999
August 16, 2005
August 1994
 
  • Drug use
  • Opioid withdrawal
  • Opioid agonist effects
  • Dose choice
Same as current
Complete list of historical versions of study NCT00000227 on ClinicalTrials.gov Archive Site
 
 
 
Alternate-Day Buprenorphine Administration. Phase VIII - 9
Alternate-Day Buprenorphine Administration. Phase VIII

The purpose of this study is to evaluate open buprenorphine dosing with dose choice.

 
Phase II
Interventional
Treatment, Placebo Control, Crossover Assignment
Opioid-Related Disorders
Drug: Buprenorphine
 
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Completed
0
 
 

Please contact site for information.

Both
25 Years to 48 Years
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00000227
 
NIDA-06969-9, R01-06969-9
National Institute on Drug Abuse (NIDA)
University of Vermont
Principal Investigator: Warren Bickel, Ph.D. University of Vermont
National Institute on Drug Abuse (NIDA)
July 1996

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP