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A Study for Assessing Treatment of Patients Ages 10-17 With Bipolar Depression

2014-08-27 03:24:15 | BioPortfolio

Summary

The main goal of this study is to help answer the following research question(s) and not to treat the child's illness.

- Can this study drug make children with bipolar depression feel better?

- Does this study drug work better than a placebo (sugar pill)?

- Does this study drug cause side effects in children who take it?

- Is this drug safe to use in children? (The study drug is a mixture of olanzapine and fluoxetine)

Study Design

Allocation: Randomized, Control: Placebo Control, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Conditions

Bipolar Depression

Intervention

Olanzapine Fluoxetine Combination, Placebo

Location

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559)
San Diego
California
United States
92123

Status

Recruiting

Source

Eli Lilly and Company

Results (where available)

View Results

Links

Published on BioPortfolio: 2014-08-27T03:24:15-0400

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