Viewing Study NCT00106405



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Last Modification Date: 2024-10-26 @ 9:11 AM
Study NCT ID: NCT00106405
Status: COMPLETED
Last Update Posted: 2012-03-05
First Post: 2005-03-24

Brief Title: An Evaluation of the Safety and Efficacy of Memantine in Patients With Acute Mania Associated With Bipolar I Disorder
Sponsor: Forest Laboratories
Organization: Forest Laboratories

Study Overview

Official Title: A Pilot Evaluation of the Safety and Efficacy of Memantine in Patients With Acute Mania Associated With Bipolar I Disorder
Status: COMPLETED
Status Verified Date: 2012-03
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Bipolar disorder affects 24 million adults in the USA between the ages of 18-65 and has considerable economic impact on our society Bipolar mania accounts for 1 in 7 psychiatric emergencies and is associated with significant morbidity and mortality The purpose of the study is to evaluate the safety and efficacy of open-label memantine in the acute management of adults with bipolar I disorder hospitalized for mania
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