Adjunctive Lisdexamfetamine (LDX) in Bipolar Depression
Stopped early · Phase 3 · Has a placebo group
Conditions studied: Bipolar, Depression
In brief
The specific aim of this study is to evaluate the efficacy and tolerability of lisdexamfetamine in the adjunctive treatment of bipolar disorder.
Key facts
- Study ID
- NCT01131559
- Run by
- Lindner Center of HOPE
- People needed
- 50
- Starts
- 2010-01-01
- Expected to finish
- 2014-02-01
- Last updated by the study team
- 2014-03-05
Who can join
Age: 18 and older, up to 55. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Subjects will meet DSM-IV-TR criteria bipolar I or II disorder,
You may not qualify if…
- Women who are pregnant, lactating, or of childbearing potential who are not using adequate contraceptive measures.
- Clinically unstable medical disease, including cardiovascular, hepatic, renal, gastrointestinal, pulmonary, metabolic, endocrine or other systemic disease. Subjects should be biochemically euthyroid to enter the study.
Where it is running
- Lindner Center of HOPE — Mason, Ohio, United States
Full record on ClinicalTrials.gov
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