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A Neuroimaging and Epigenetic Investigation of Antidepressants in Depression

A Neuroimaging and Epigenetic Investigation of Antidepressants in Depression

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00703742
Enrollment
200
Registered
2008-06-23
Start date
2008-06-30
Completion date
2011-06-30
Last updated
2019-09-17

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

Conditions

Depression, Depression Secondary to Other Disease

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

Interventions

DRUGEscitalopram

A,1: Escitalopram, oral, 20 mg/day, 8 weeks

Sponsors

Chinese Academy of Sciences
CollaboratorOTHER_GOV
Kunming Medical University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
Yes

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 * Pregnant * High suicide risk * Currently taking (within 2 weeks; 4 weeks for Fluoxetine) antidepressants

Design outcomes

Primary

MeasureTime frame
change of fMRI after medicationbaseline, 4 weeks, 8 weeks

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 27, 2026