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CompletedNCT00566020

Long-term lamotrigine safety in bipolarity type I

About this title

A Clinical Evaluation Of BW430C (Lamotrigine) In Bipolar I Disorder- Long-term Extension Of Study SCA104779 (NCT00550407) -

Read the official source — NCT00566020
Medication studyAges 20+Japan
The study in practice

Understand this study

Who was this study for?

This study was for people with bipolarity. Listed age limits: from 20 years. Other eligibility criteria applied.

Listed locations
Aichi and 51 more locationsSee all locations and recruitment
Study phase
Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.
Study clarity

Study information

Study start dateMay 2008
Recruitment status
Completed
Enrollment listed in the registry
92
Sponsor
GlaxoSmithKline
Sponsor type
Unknown or unclear
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
Japan
Age range
Over 20 Years
Official registry ID
NCT00566020
Official title
Show the full official title

Study SCA106052, a Clinical Evaluation of BW430C (Lamotrigine) in Bipolar I Disorder- Long-term Extension Study (Extension of Study SCA104779 (NCT00550407))

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Recruitment & locations

Completed

Aichi · Chiba · Fukuoka

17 more locations
  • Gunma
  • Hiroshima
  • Hokkaido
  • Ibaraki
  • Kanagawa
  • Kumamoto
  • Kyoto
  • Mie
  • Nara
  • Okayama
  • Osaka
  • Ōita
  • Saga
  • Saitama
  • Tokyo
  • Tottori
  • Yamagata
FAQ

Questions about this study

Who is behind this study?

The study sponsor is GlaxoSmithKline.

Did this study involve medication?

Yes. The study involved medication, including BW430C (lamotrigine).

Who was this study for?

This study was for people with bipolarity. Listed age limits: from 20 years. Other eligibility criteria applied.

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