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A prediction study of antidepressant treatment effect on major depressive disorder based neuroimaging features of the prefrontal-limbic circuit

A prediction study of antidepressant treatment effect on major depressive disorder based neuroimaging features of the prefrontal-limbic circuit

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100047520
Enrollment
Unknown
Registered
2021-06-20
Start date
2021-06-15
Completion date
Unknown
Last updated
2022-02-21

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

Conditions

Major depressive disorder(MDD)

Interventions

Test group:Selective Serotonin Reuptake Inhibitor (SSRI)

Sponsors

Beijing Anding Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Out-patients, male or female, aged 18 to 65 years; 2. Meet the diagnosis standard of DSM-IV/MINI, first episode or recurrence, current episode depressed without psychotic features; 3. Did not under anti depressive treatment or cumulative treatment no more than 7 days; 4. Having 17-item Hamilton Depression Rating Scale (HAMD-17) total score = 14; 5. Primary school or above education background, to be able to understand the content of the questionaire; 6. No contraindications for MRI; 7. Signed informed consent.

Exclusion criteria

Exclusion criteria: 1. A history of mania or hypomania; 2. Any preexisting or concurrent co-morbid primary diagnoses that met the DSM-IV criteria for any Axis I disorder other than MDD, such as schizophrenia or bipolar disorders; 3. Have alcohol/drug dependence or acute poisoning; 4. Pregnant or lactating women; 5. Currently have a serious risk of suicide judged by investigators, suicide item of HAMD-17 score = 3; 6. Currently have severe physical illnesses which researchers think it is risky and not eligible to participate; 7. Unable to tolerate or failed to SSRI.

Design outcomes

Secondary

MeasureTime frame
Remission rate;

Primary

MeasureTime frame
The change of HAMD-17 total score;Difference of neuroimaging feature;

Countries

China

Contacts

Public ContactLiu Rui

Beijing Anding Hospital, Capital Medical University

ruiliu@ccmu.edu.cn+86 15105179161

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026