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Neuroimaging Studies of the Treatment of Bipolar Depression With Citalopram

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Mass General Brigham

Status

Completed

Conditions

Bipolar Depression

Study type

Observational

Funder types

Other

Identifiers

NCT01639482
2009P002712

Details and patient eligibility

About

Regional metabolic changes associated with response to 6 weeks of citalopram treatment, using 18-Fluorodeoxyglucose Positron Emission Tomography imaging, will be characterized (FDG PET).

Full description

Regional metabolic changes associated with response to 6 weeks of citalopram treatment, using 18-Fluorodeoxyglucose Positron Emission Tomography imaging, will be characterized (FDG PET). The following hypothesis will be tested: Antidepressant response or remission in depressed BPD patients will be associated with changes in cortical (prefrontal, parietal, premotor) and paralimbic (hippocampus, anterior cingulate, subgenual cingulate, posterior cingulate, and anterior insula) regions, consistent with SRI antidepressant response in unipolar depressed patients.

Enrollment

60 patients

Sex

All

Ages

18 to 64 years old

Volunteers

No Healthy Volunteers

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

Trial design

60 participants in 2 patient groups

Citalopram
Description:
Patients with bipolar disorder
Placebo
Description:
Patients with bipolar disorder

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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