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Development of Pharmacogenomic Method to Predict Antidepressant Responsiveness — PG  

Depression Clinical Trial

Official title:
Phase 4 Study of Development of Pharmacogenomic Method to Predict Antidepressant Responsiveness

Clinical Trial Summary

The Purpose of this study is to predict antidepressant response in advance using pharmacogenomics and peripheral biological markers in depressed patients.

Clinical Trial Description

The difficulties to treat depressed patients are 1)the patients don't respond to antidepressant is about 40% of which, and 2) The time lag is existed until the patients respond to antidepressant and show the treatment effects.

If it is predicted the response of antidepressant in advance, it would be overcome such problems. Drug response generally is known to be related to the individual genetic information and the environmental factors. We are going to investigation about antidepressant response using these approaches. ;

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

  • Antidepressant Drug Adverse Reaction
  • Depression
  • Drug-Related Side Effects and Adverse Reactions
Clinical Trial Details
NCT number NCT00817011
Study type Interventional
Source Samsung Medical Center
Contact Doh Kwan Kim, M.D.,Ph.D
Phone 82-2-3410-0946
Email jungshil.back@sbri.co.kr
Status Recruiting
Phase N/A
Start date April 2006
Completion date March 2018
View Details
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