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Temporal Discounting Delayed Outcomes on Opioid-Dependent Outpatients - 20
This study has been completed.
Study NCT00000238   Information provided by National Institute on Drug Abuse (NIDA)
First Received: September 20, 1999   Last Updated: November 19, 2008   History of Changes

September 20, 1999
November 19, 2008
August 1997
 
  • Drug use
  • Money choice
  • Heroin craving
Same as current
Complete list of historical versions of study NCT00000238 on ClinicalTrials.gov Archive Site
 
 
 
Temporal Discounting Delayed Outcomes on Opioid-Dependent Outpatients - 20
Temporal Discounting Delayed Outcomes on Opioid-Dependent Outpatients

The purpose of this study is to assess the degree in which opioid-dependent outpatients discount the value of an additional maintenance dose of buprenorphine under differing states of opioid deprivation.

 
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
 
 

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Both
18 Years to 47 Years
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00000238
 
NIDA-06969-20, R01-06969-20
National Institute on Drug Abuse (NIDA)
University of Vermont
Principal Investigator: Warren Bickel, Ph.D. University of Vermont
National Institute on Drug Abuse (NIDA)
November 2008

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