Viewing Study NCT00146471



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Last Modification Date: 2024-10-26 @ 9:14 AM
Study NCT ID: NCT00146471
Status: COMPLETED
Last Update Posted: 2009-12-30
First Post: 2005-09-06

Brief Title: Efficacy and Safety of Levetiracetam in the Inpatient Treatment of Alcohol Withdrawal Syndrome
Sponsor: Charite University Berlin Germany
Organization: Charite University Berlin Germany

Study Overview

Official Title: Efficacy and Safety of Levetiracetam in the Inpatient Treatment of Alcohol Withdrawal Syndrome Sicherheit Und Wirksamkeit Von Levetiracetam Keppra für Die Behandlung Des stationären Alkoholentzugsyndroms
Status: COMPLETED
Status Verified Date: 2008-09
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief 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
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None