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Clinical Trials/NCT00703742
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:

  1. to find out the structural or functional effects of selective serotonin reuptake inhibitors (SSRI) in major depressive disorder (MDD);
  2. find special abnormalities in depression secondary to other disease, e.g., autoimmune disease like systemic lupus erythematosus (SLE).
  3. find the relationship between the efficacy of antidepressant and the change of neuroimaging in MDD
  4. to find possible predispose to MDD
  5. 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

Registry
clinicaltrials.gov
Start Date
June 2008
End Date
June 2011
Last Updated
6 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Kunming Medical University
Responsible Party
Principal Investigator
Principal Investigator

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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