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Alternate-Day Buprenorphine. Phase V - 6
This study has been completed.
Study NCT00000224   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
February 1993
 
  • Drug use
  • Opioid withdrawal
  • Subjective dose estimate
  • Drug effect characteristics: ARCI
  • Physiological changes in: pupil diameter
  • Physiological changes in: blood pressure
  • Physiological changes in: heart rate
  • Physiological changes in: respiration
  • Physiological changes in: bup plasma levels
Same as current
Complete list of historical versions of study NCT00000224 on ClinicalTrials.gov Archive Site
 
 
 
Alternate-Day Buprenorphine. Phase V - 6
Alternate-Day Buprenorphine. Phase V

The purpose of this study is to evaluate buprenorphine blockade challenge.

 
Phase I
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
30 Years to 49 Years
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00000224
 
NIDA-06969-6, R01-06969-6
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 1996

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