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Alternate-Day Buprenorphine Administration. Phase VII - 8
This study has been completed.
Study NCT00000226   Information provided by National Institute on Drug Abuse (NIDA)
First Received: September 20, 1999   Last Updated: June 23, 2005   History of Changes

September 20, 1999
June 23, 2005
November 1994
 
  • Drug use
  • Opioid withdrawal
  • Opioid agonist effects
  • Pupil diameter
Same as current
Complete list of historical versions of study NCT00000226 on ClinicalTrials.gov Archive Site
 
 
 
Alternate-Day Buprenorphine Administration. Phase VII - 8
Alternate-Day Buprenorphine Administration. Phase VII

The purpose of this study is to determine if four times a subjects daily maintenance dose will hold for 96 hours without changes in agonist and antagonist effects under open dosing conditions.

 
Phase II
Interventional
Treatment
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
21 Years to 48 Years
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00000226
 
NIDA-06969-8, R01-06969-8
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