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CompletedNCT02731612

Lurasidone for Cognitive Symptoms in Bipolarity

About this titleRead the official source — NCT02731612

This study evaluated the effectiveness of lurasidone for people with bipolarity.

Medication studyAges 19–65Multiple countries
The study in practice

Understand this study

What did researchers investigate?

This study evaluated the effectiveness of lurasidone for people with bipolarity.

Who was this study for?

Listed age limits: 19 years to 65 years.

Listed locations
Boston and 8 more locationsSee all locations and recruitment
Study phase
Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.

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Study clarity

Study information

Study start dateStarted: May 8, 2017
Recruitment status
Completed
Enrollment listed in the registry
100
Sponsor
Lakshmi N Yatham
Sponsor type
Individual investigator
Study type
Drug
Intervention type
Drug, Other
Study phase
Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.
Locations
United States, Canada, United Kingdom, ...
Age range
From 19 Years to 65 Years
Official registry ID
NCT02731612
Official title
Show the full official title

A 6-Week Randomised, Double-Blind, Placebo-Controlled, Multicenter Study to Evaluate the Efficacy of Lurasidone Adjunctive Therapy in Improving Cognitive Functioning in Euthymic Bipolar Disorder Patients (ELICE-BD)

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Recruitment & locations

Completed

Boston, United States · Cleveland, United States · Vancouver, Canada

6 more locations
  • Kitakyushu, Japan
  • Moriguchi-shi, Japan
  • Kita-ku, Japan
  • Kodaira, Japan
  • Aichi, Japan
  • London, United Kingdom

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FAQ

Questions about this study

What did researchers investigate?

This study evaluated the effectiveness of lurasidone for people with bipolarity.

Who is behind this study?

The study sponsor is Lakshmi N Yatham.

Did this study involve medication?

Yes. The study involved medication, including lurasidone.

Who was this study for?

Listed age limits: 19 years to 65 years.

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