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Oral and Depot Naltrexone - 1 - Article


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Heroin

 




Clinical Trial: Oral and Depot Naltrexone - 1

This study is not yet open for patient recruitment.
Verified by National Institute on Drug Abuse (NIDA) September 2005

Sponsored by: National Institute on Drug Abuse (NIDA)
Information provided by: National Institute on Drug Abuse (NIDA)
ClinicalTrials.gov Identifier: NCT00218426

Purpose

The purpose of this study is to compare a six month course of oral naltrexone with a six month course of depot naltrexone for relapse prevention to heroin addiction in St. Petersburg, Russia.
Condition Intervention Phase
Heroin Dependence
 Drug: Depot naltrexone
Phase II
Phase III

MedlinePlus related topics:  Heroin

Study Type: Interventional
Study Design: Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Efficacy Study

Official Title: Addiction Treatment in Russia: Oral and Depot Naltrexone

Further Study Details: 
Primary Outcomes: Relapse to heroin addiction

Study start: January 2006

Eligibility

Ages Eligible for Study:  18 Years   -   50 Years,  Genders Eligible for Study:  Both
Criteria

Inclusion Criteria:

  • Current opioid dependence, having recently completed detoxification
  • Not planning leaving the area within the 12 months following enrollment

Exclusion Criteria:

  • Pregnancy
  • Serious medical or psychiatric conditions requiring immediate hospitalization or that would make participation in study hazardous
  • Planning to leave the area within the next 12 months
  • Imminent incarceration

Location and Contact Information

Please refer to this study by ClinicalTrials.gov identifier  NCT00218426


Pennsylvania
      University of Pennsylvania, Philadelphia,  Pennsylvania,  19104 6178,  United States
George Woody, M.D.  215-399-0980  Ext. 112    woody@tresearch.org 

Russian Federation
      Pavlov Medical University, St Petersburg,  197022,  Russian Federation
Evgeny Krupitsky, M.D., Ph.D.  (203)932-5711  Ext. 7438 

Study chairs or principal investigators

George Woody, M.D.,  Principal Investigator,  University of Pennsylvania   

More Information

Study ID Numbers:  NIDA-17317-1; R01-17317-1
Last Updated:  September 21, 2005
Record first received:  September 16, 2005
ClinicalTrials.gov Identifier:  NCT00218426
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-09-27

Resources



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Page Updated: October 3, 2005
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