drugset / Trial / NCT00146471

Efficacy and Safety of Levetiracetam in the Inpatient Treatment of Alcohol Withdrawal Syndrome

NCT00146471

Phase 3 Completed 120 enrolled Charite University, Berlin, Germany
RandomizedParallel-groupTriple-blindTreatment

Summary

The purpose of this study is to evaluate the efficacy and safety of levetiracetam for treating alcohol withdrawal syndrome (AWS) in inpatients (vs. placebo). The primary come-out parameter is the reduction of the total needed amount of diazepam for add-on treatment of acute alcohol withdrawal symptoms. The secondary come-out parameter are - safety criteria (AE) - reduction of alcohol withdrawal score over the days.

Timeline

Start
2006-01
Primary completion
2007-07
Completion
2007-09

Drugs

EvaluationDrugModalityDoseRoute
Comparator Levetiracetam Other / unclassified 1500 mg
Comparator Levetiracetam Other / unclassified 2000 mg

Indications