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CompletedNCT00199966

Divalproex extended release for bipolarity in children and adolescents

About this title

Safety And Efficacy Study Of Depakote ER To Treat Pediatric Bipolar Disorder

Read the official source — NCT00199966
Medication studyAges 6–17United States
The study in practice

Understand this study

Who was this study for?

Listed age limits: 6 years to 17 years.

Listed locations
MilwaukeeSee all locations and recruitment
Study phase
Phase 4Usually happens after approval, to monitor real-world use, safety, and longer-term outcomes.

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Study clarity

Study information

Study start dateDecember 2003
Recruitment status
Completed
Enrollment listed in the registry
30
Sponsor
Medical College of Wisconsin
Sponsor type
University
Study type
Drug
Intervention type
Drug
Study phase
Phase 4Usually happens after approval, to monitor real-world use, safety, and longer-term outcomes.
Locations
United States
Age range
From 6 Years to 17 Years
Official registry ID
NCT00199966
Official title
Show the full official title

A Pilot Study Of Safety And Effectiveness For Depakote ER In Pediatric Bipolar Disorder

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Recruitment & locations

Completed

Milwaukee

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FAQ

Questions about this study

Who is behind this study?

The study sponsor is Medical College of Wisconsin, a university.

Did this study involve medication?

Yes. The study involved medication, including Divalproex sodium extended release.

Who was this study for?

Listed age limits: 6 years to 17 years.

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