Neuroimaging Studies of the Treatment of Bipolar Depression With Citalopram
Completed
Conditions studied: Bipolar Depression
In brief
Regional metabolic changes associated with response to 6 weeks of citalopram treatment, using 18-Fluorodeoxyglucose Positron Emission Tomography imaging, will be characterized (FDG PET).
Key facts
- Study ID
- NCT01639482
- Run by
- Massachusetts General Hospital
- People needed
- 60
- Starts
- 2010-04-01
- Expected to finish
- 2013-12-01
- Last updated by the study team
- 2019-03-07
Who can join
Age: 18 and older, up to 64. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Current age 18-64 years; DSM-IV diagnosis of BPD, type-I, or type-II; Enrolled in the Citalopram Study at Tufts Medical Center
You may not qualify if…
- Current pregnancy, or inability to utilize contraception, The presence of any metallic implants, History of claustrophobia
Where it is running
- Massachusetts General Hospital - East — Charlestown, Massachusetts, United States
Full record on ClinicalTrials.gov
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