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Pharmacogenomic Study to Predict Antidepressant Responsiveness in Depressed Patients

Depression Clinical Trial

Official title:
Pharmacogenomic Study to Predict Antidepressant Responsiveness in Depressed Patients

Clinical Trial Summary

The purpose of this study is to determine whether pharmacogenomic study predict antidepressant responsiveness in advance before the appearance of the drug effects until 4~6 weeks after drug administration.

Clinical Trial Description

The purpose of this study is

1. to determine whether genomic effects on antidepressant response differed by class of drug,

2. whether genomic differences between drug responders and nonresponders predict the response of antidepressant and

3. to construct the prediction model for antidepressant treatment in order to aid to select the their genetically matching drugs. ;

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00817375
Study type Interventional
Source Samsung Medical Center
Contact JungShil Back, B/Sc.
Phone 82-2-3410-0946
Email jungshil.back@sbri.co.kr
Status Recruiting
Phase N/A
Start date February 2003
Completion date December 2018
View Details
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