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Antiglutamate Anticonvulsants in the Treatment of Alcohol Withdrawal Syndrome

This study has been completed.

Sponsored by: St. Petersburg State Pavlov Medical University
Information provided by: St. Petersburg State Pavlov Medical University
ClinicalTrials.gov Identifier: NCT00241995
  Purpose

The study is aimed to evaluate the efficacy of antiglutamate anticonvulsants (topiramate, lamotrigine, and memantine) in the treatment of alcohol withdrawal syndrome


Condition Intervention
Topiramate
Lamotrigine
Memnatine
Diazepam
Placebo
Drug: Anticonvulsants

ChemIDplus related topics:   Ethanol   

U.S. FDA Resources

Study Type:   Interventional
Study Design:   Treatment, Randomized, Single Blind, Placebo Control, Parallel Assignment, Efficacy Study
  Eligibility
Ages Eligible for Study:   20 Years to 60 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes

Criteria

Inclusion Criteria:

Alcohol dependence Alcohol withdrawal syndrome

Exclusion Criteria:

Drug dependence Major psychiatric diagnoses Severe somatic illness

  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00241995

Sponsors and Collaborators
St. Petersburg State Pavlov Medical University

Investigators
Principal Investigator:     Evgeny M Krupitsky, MD, PhD     St. Petersburg State Pavlov Medical University    
  More Information


Study ID Numbers:   RCT-RCT_LOND_GAT_AWS_2003
First Received:   October 17, 2005
Last Updated:   October 17, 2006
ClinicalTrials.gov Identifier:   NCT00241995
Health Authority:   Russia: Ministry of Health and Social Development of the Russian Federation

Study placed in the following topic categories:
Substance Withdrawal Syndrome
Ethanol

ClinicalTrials.gov processed this record on October 17, 2008




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