NCT00703742
Completed
Not Applicable
A Neuroimaging and Epigenetic Investigation of Antidepressants in Depression
Kunming Medical University1 site in 1 country200 target enrollmentJune 2008
Overview
- Phase
- Not Applicable
- Intervention
- Escitalopram
- Conditions
- Depression
- Sponsor
- Kunming Medical University
- Enrollment
- 200
- Locations
- 1
- Primary Endpoint
- change of fMRI after medication
- Status
- Completed
- Last Updated
- 6 years ago
Overview
Brief Summary
The purpose of this study is:
- to find out the structural or functional effects of selective serotonin reuptake inhibitors (SSRI) in major depressive disorder (MDD);
- find special abnormalities in depression secondary to other disease, e.g., autoimmune disease like systemic lupus erythematosus (SLE).
- find the relationship between the efficacy of antidepressant and the change of neuroimaging in MDD
- to find possible predispose to MDD
- to explore the DNA methylation status in depression;
Detailed Description
1. to explore the pathology of depression 2. to identify the difference between MDD and depression secondary to other disease ,especially autoimmune disease 3. to explore the effect of gene-environment interaction on the epigenetic regulation of the depression
Investigators
Yuqi Cheng
Vise director, psychiatry department, Kunming Medical University
Kunming Medical University
Eligibility Criteria
Inclusion Criteria
- •DSM-IV Major Depression or Dysthymia
- •Age 18-65
- •Physically healthy
- •Drug-free
Exclusion Criteria
- •Body metal (e.g., wire stitches, screws in bones, stainless steel hips)
- •History of Psychosis or Epilepsy
- •Current (past six months) Substance Use Disorder (illicit drugs and/or alcohol)
- •Bipolar I
- •Need for wash-out from effective treatment in order to participate
- •High suicide risk
- •Currently taking (within 2 weeks; 4 weeks for Fluoxetine) antidepressants
Arms & Interventions
A,1
A: Escitalopram, 20 mg/day,8weeks
Intervention: Escitalopram
Outcomes
Primary Outcomes
change of fMRI after medication
Time Frame: baseline, 4 weeks, 8 weeks
Study Sites (1)
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