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Predict Antidepressant Responsiveness Using Pharmacogenomics

Predict Antidepressant Responsiveness Using Pharmacogenomics

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01228357
Enrollment
1000
Registered
2010-10-26
Start date
2003-02-28
Completion date
2018-12-31
Last updated
2015-12-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Depression, Depressive Symptoms

Keywords

Pharmacogenomics, Depressed Patients

Brief summary

The purpose of this study is to determine whether genetic information associated with individual depressive symptoms.

Detailed description

The primary hypothesis is that the variations of the candidate genes are associated with individual symptoms in patients with depression. The Second hypothesis is that patients with the associated genetic variation suffer longer from the associated symptom than the patients without the associated genetic variation.

Interventions

Antidepressant administration of SSRI class for 12 weeks under therapeutic dose

Antidepressant administration of non-SSRI class for 12 weeks under therapeutic dose

Sponsors

Samsung Medical Center
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
19 Years to 89 Years
Healthy volunteers
Yes

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.

Design outcomes

Primary

MeasureTime frameDescription
Presences of each individual symptom of depression at 1,2,4,6,12 weeks12 weeks17-items HAM-D scale was employed to measure depressive symptoms

Countries

South Korea

Contacts

Primary ContactJungShil Back, B/Sc.
jungshil.back@sbri.co.kr82-2-3410-0946
Backup ContactShinn-Won Lim, phD
shinwon.lim@sbri.co.kr82-2-3410-3759

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026