Citalopram
DrugPDA Approved antidepressant
NCT Number: NCT00047671
This 11-week study aims to determine how genetic factors affect the way African Americans and Caucasians with major depression respond to antidepressant medication [citalopram (Celexa®)].
Looking for future studies?
Notify Me18 year–70 year
All sexes
Interventional
Phase 4
Cedars-Sinai Medical Center, Department of Psychiatry, Clinical Trials Unit, Los Angeles, California, United States
Depressed patients vary substantially in their responses to antidepressants. Genetic factors may account for a large part of these differences in response. This study will include both African Americans and Caucasians to examine the role of genetic factors in treatment response.
Participants receive citalopram (Celexa) for 8 weeks and a placebo for 1 week. Visits occur once a week for 11 weeks. A variety of interviews, scales, tests, and questionnaires are used to assess participants.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
PDA Approved antidepressant
Time frame: Measured weekly for 11 weeks
Looking for future studies?
Notify MeNational Institute of Mental Health (NIMH)
Nih
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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