Skip to main content
Clinical Trials/NCT01237275
NCT01237275
Unknown
Not Applicable

Development of A Technique to Predict Antidepressant Responsiveness in Depressive Patients

Samsung Medical Center1 site in 1 country300 target enrollmentOctober 1999

Overview

Phase
Not Applicable
Intervention
SSRI treated group
Conditions
Depression
Sponsor
Samsung Medical Center
Enrollment
300
Locations
1
Primary Endpoint
Antidepressant Response at 2,4,6 weeks
Last Updated
10 years ago

Overview

Brief Summary

First, the investigators examined the functional relevance of serotonin transporter polymorphisms by quantifying the activity of serotonin transporter in blood platelets of genotyped healthy volunteers and patients with major depression.

Second, the investigators studied response to SSRIs in relation to 5-HTTLPR genotype and also to the functional expression of 5-HTT in platelets.

Detailed Description

The purpose of this study is 1. to determine whether serotonin transporter genotypic or functional differences between depressive patients and normal controls were existed. 2. to determine the relationship between serotonin transporter polymorphisms and serotonin transporter functional expression. 3. to determine whether genomic or functional differences between drug responders and nonresponders predict the response of antidepressant

Registry
clinicaltrials.gov
Start Date
October 1999
End Date
December 2016
Last Updated
10 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Doh Kwan Kim

M.D.,Ph.D.

Samsung Medical Center

Eligibility Criteria

Inclusion Criteria

  • Eligible patients were enrolled in the clinical trials program of hte Samsung Medical Center Geropsychiatry and Affective Disorder Clinics(Seoul, Korea). They received a semistructured diagnostic interview, the Samsung Psychiatric Evaluation Schedule. The affective disorder section of the Samsung Psychiatric Evaluation Schedule uses the Korean version of the structured clinical interview for the diagnostic and statistical manual of mental disorders, Fourth edition.
  • interview with one more patient's family member for objective diagnosis and final diagnosis decision by agreements of two more psychiatric physicians

Exclusion Criteria

  • received psychotropic medication within 2 weeks of the study or fluoxetine within 4 weeks
  • potential study participants for pregnancy, significant medical conditions, abnormal laboratory baseline values, unstable psychiatric features(eg.suicidal), history of alcohol of drug dependence, seizures, head trauma with loss of consciousness, neurological illness, or concomitant Axis I psychiatric disorder.

Arms & Interventions

SSRI treated group

SSRI treated group are depressive patients treated with fluoxetine, paroxetine or sertraline

Intervention: SSRI treated group

Outcomes

Primary Outcomes

Antidepressant Response at 2,4,6 weeks

Time Frame: 6 weeks

Secondary Outcomes

  • Biological value at 0 and 6 weeks(6weeks)

Study Sites (1)

Loading locations...

Similar Trials