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| Sponsor: | 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 |
| 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 |
Inclusion Criteria:
Alcohol dependence Alcohol withdrawal syndrome
Exclusion Criteria:
Drug dependence Major psychiatric diagnoses Severe somatic illness
Contacts and Locations More Information
| Study ID Numbers: | RCT-RCT_LOND_GAT_AWS_2003 |
| Study First Received: | October 17, 2005 |
| Last Updated: | October 17, 2006 |
| ClinicalTrials.gov Identifier: | NCT00241995 History of Changes |
| Health Authority: | Russia: Ministry of Health and Social Development of the Russian Federation |
|
Therapeutic Uses Central Nervous System Agents Pharmacologic Actions Anticonvulsants |
