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Evaluation of Lofexidine for Treatment of Opioid Withdrawal - 3
This study has been completed.
Study NCT00000354   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
July 1996
 
 
 
Complete list of historical versions of study NCT00000354 on ClinicalTrials.gov Archive Site
 
 
 
Evaluation of Lofexidine for Treatment of Opioid Withdrawal - 3
Safety Evaluation of Lofexidine for Treatment of Opioid Withdrawal

The purpose of this study is to determine the safety of lofexidine in the treatment of opiate withdrawal. Preliminary data will also be obtained to assess the ability of lofexidine to alleviate opiate withdrawal signs and symptoms.

 
Phase I
Interventional
Treatment
  • Opioid-Related Disorders
  • Substance-Related Disorders
Drug: Lofexidine
 
 

*   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
21 Years to 59 Years
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00000354
 
NIDA-3-0012-3, Y01-3-0012-3
National Institute on Drug Abuse (NIDA)
University of Pennsylvania
Principal Investigator: Charles O'Brien, M.D., Ph.D. PDVAMC Treatment Research Center
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