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CompletedNCT00240721

A Study of the Effectiveness and Safety of Topiramate in the Treatment of Patients With Bipolarity

This study evaluated the safety and effectiveness of topiramate for people with bipolarity.

Medication studyAges 16+
The study in practice

Understand this study

What did researchers investigate?

This study evaluated the safety and effectiveness of topiramate for people with bipolarity.

Who was this study for?

This study was for people with bipolarity. Listed age limits: from 16 years. Other eligibility criteria applied.

Study phase
Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.
Study clarity

Study information

Study start dateOctober 2000
Recruitment status
Completed
Enrollment listed in the registry
363
Sponsor
Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
Sponsor type
Pharmaceutical company
Study type
Drug
Intervention type
Medication / drug
Study phase
Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.
Locations
Not clearly listed
Age range
Over 16 Years
Official registry ID
NCT00240721
Official title
Show the full official title

A Randomized, Double-Blind, Multicenter, Placebo-Controlled 12-Week Study Of The Safety And Efficacy Of Two Doses Of Topiramate For The Treatment Of Acute Manic Or Mixed Episodes In Subjects With Bipolar I Disorder With An Optional Open-Label Extension

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Recruitment & locations

Completed

Locations not listed

FAQ

Questions about this study

What did researchers investigate?

This study evaluated the safety and effectiveness of topiramate for people with bipolarity.

Who is behind this study?

The study sponsor is Johnson & Johnson Pharmaceutical Research & Development, L.L.C., a pharmaceutical company.

Did this study involve medication?

Yes. The study involved medication, including topiramate.

Who was this study for?

This study was for people with bipolarity. Listed age limits: from 16 years. Other eligibility criteria applied.

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