Viewing Study NCT00175955



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Last Modification Date: 2024-10-26 @ 9:16 AM
Study NCT ID: NCT00175955
Status: COMPLETED
Last Update Posted: 2013-12-06
First Post: 2005-09-09

Brief Title: Levetiracetam in the Treatment of Neuroleptic-induced Tardive Dyskinesia
Sponsor: UCB Pharma
Organization: UCB Pharma

Study Overview

Official Title: An 8-week Exploratory Double-blind Placebo Controlled Randomized Trial Evaluation of the Efficacy and Safety of Levetiracetam up to 3000 mgDay 250-500 mg Oral Tablets in bid Administration on Neuroleptic-induced Tardive Dyskinesia in Subjects With Stable Axis I Psychiatric Disorder Aged From at Least 18 Years to 80 Years
Status: COMPLETED
Status Verified Date: 2009-09
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: An 8-week study to examine safety and efficacy of levetiracetam in patients with neuroleptic-induced tardive dyskinesia
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
Secondary IDs
Secondary ID Type Domain Link
EudraCT Number 2004-001302-27 None None None