Bipolar Depression Clinical Trial
Official title:
Neuroimaging Studies of the Treatment of Bipolar Depression With Citalopram
NCT number | NCT01639482 |
Other study ID # | 2009P002712 |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | April 2010 |
Est. completion date | December 2013 |
Verified date | March 2019 |
Source | Massachusetts General Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
Regional metabolic changes associated with response to 6 weeks of citalopram treatment, using 18-Fluorodeoxyglucose Positron Emission Tomography imaging, will be characterized (FDG PET).
Status | Completed |
Enrollment | 60 |
Est. completion date | December 2013 |
Est. primary completion date | December 2013 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 64 Years |
Eligibility |
Inclusion Criteria: - Current age 18-64 years; DSM-IV diagnosis of BPD, type-I, or type-II; Enrolled in the Citalopram Study at Tufts Medical Center Exclusion Criteria: - Current pregnancy, or inability to utilize contraception, The presence of any metallic implants, History of claustrophobia |
Country | Name | City | State |
---|---|---|---|
United States | Massachusetts General Hospital - East | Charlestown | Massachusetts |
Lead Sponsor | Collaborator |
---|---|
Massachusetts General Hospital |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | rCMRglu | regional glucose metabolism | pre and post-treatment |
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