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A prospective cohort study on factors associated with treatment effect in major depressive disorder

A prospective cohort study on factors associated with treatment effect in major depressive disorder

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000033402
Enrollment
Unknown
Registered
2020-05-31
Start date
2020-06-15
Completion date
Unknown
Last updated
2020-06-01

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

Conditions

major depressive disorder

Interventions

Healthy control group:none

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 60 Years

Inclusion criteria

Inclusion criteria: Patient group: Under 60 years old, right-handed, elementary school or above education level, IQ> 85, head movement during MRI scan is not more than 2mm, as determined by imaging physicians, there is no organic brain structure abnormality, which is in accordance with DSM-V depression Diagnostic criteria, can understand the contents of the scale, have not received electrical convulsions, patient themselves and their family members have informed consent and voluntarily participated in this study. Healthy control group: Under 60 years old, right-handed, elementary school or above education level, IQ> 85, head movement during MRI scan is not more than 2mm, as determined by imaging doctors without organic brain structure abnormalities, can understand the scale Contents, have not taken any psychoactive drugs, have not taken any other drugs recently, have no major or chronic physical diseases, and have a negative family history of mental disorders, controls themselves and their family members have informed consent and voluntarily participated in this study.

Exclusion criteria

Exclusion criteria: Patient group: Patients with other Axis I and Axis II mental diseases, other physical diseases, neurological diseases or injuries, patients who have used psychoactive substances, pregnancy or lactation, and claustrophobia are excluded. Healthy control group: Coexisting other Axis I and Axis II mental diseases, suffering from other physical diseases, having a history of suicide attempts or a history of neurological diseases or injuries, people who have used psychoactive substances, pregnancy or lactation, and claustrophobia are excluded.

Design outcomes

Primary

MeasureTime frame
Environmental factor assessment;Magnetic Resonance Imaging;Genome-wide genetic data;intestinal flora;Blood, urine and fecal metabolites were analyzed based on omics;electroencephalogram;

Countries

China

Contacts

Public ContactYin Li

West China School of Clinical Medicine, Sichuan University

yli009@163.com+86 18980606720

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 21, 2026