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CompletedNCT00106405

Memantine for acute mania in adults with bipolarity

About this title

An Evaluation of the Safety and Efficacy of Memantine in Patients With Acute Mania Associated With Bipolar I Disorder

Read the official source — NCT00106405
Medication studyAges 18–65United States
The study in practice

Understand this study

Who was this study for?

This study was for people with bipolarity. Listed age limits: 18 years to 65 years. Other eligibility criteria applied.

Listed locations
National City and 5 more locationsSee all locations and recruitment
Study phase
Phase 2Usually explores whether the intervention may work, while continuing to monitor safety.

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Study clarity

Study information

Study start dateFebruary 2005
Recruitment status
Completed
Enrollment listed in the registry
35
Sponsor
Forest Laboratories
Sponsor type
Pharmaceutical company
Study type
Drug
Intervention type
Medication / drug
Study phase
Phase 2Usually explores whether the intervention may work, while continuing to monitor safety.
Locations
United States
Age range
From 18 Years to 65 Years
Official registry ID
NCT00106405
Official title
Show the full official title

A Pilot Evaluation of the Safety and Efficacy of Memantine in Patients With Acute Mania Associated With Bipolar I Disorder

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Recruitment & locations

Completed

National City · Baltimore · Saint Charles

3 more locations
  • Cincinnati
  • Galveston
  • Irving
FAQ

Questions about this study

Who is behind this study?

The study sponsor is Forest Laboratories, a pharmaceutical company.

Did this study involve medication?

Yes. The study involved medication, including Memantine HCl.

Who was this study for?

This study was for people with bipolarity. Listed age limits: 18 years to 65 years. Other eligibility criteria applied.

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