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Alternate Day Buprenorphine Administration, Phase IX - 14
This study has been completed.
Study NCT00000232   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
March 1992
 
  • Drug use
  • Opioid withdrawal
  • Opioid agonist effects
  • Dose identification
  • Pupil diameter
Same as current
Complete list of historical versions of study NCT00000232 on ClinicalTrials.gov Archive Site
 
 
 
Alternate Day Buprenorphine Administration, Phase IX - 14
Alternate Day Buprenorphine Administration, Phase IX

The purpose of this study is to determine if four times a subjects' daily maintenance dose will hold for 120 hours without changes in agonist and antagonist effects.

 
Phase II
Interventional
Treatment, Double-Blind, 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
22 Years to 51 Years
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00000232
 
NIDA-06969-14, R01-06969-14
National Institute on Drug Abuse (NIDA)
University of Vermont
Principal Investigator: Warren Bickel, Ph.D. University of Vermont
National Institute on Drug Abuse (NIDA)
April 1994

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