About this trial
This project aims to investigate the effectiveness of existing common antidepressants and to provide new evidence for depressed children and adolescents who are not responding to their first treatment.
Eligibility criteria
Qualifiers
Age 13 - 18
As assessed by K-SADS-PL, it meets the DSM-V criteria for MDD with non-psychotic symptoms
Score≥40 on the CDRS-R
Participants with suicidal ideation are eligible, as long as clinicians consider outpatient treatment to be safe
Disqualifiers
History of bipolar disorder, schizophrenia, autism, eating disorders, primary obsessive compulsive disorder, pervasive developmental disorder, or psychosis not otherwise specified
History of serious physical illnesses
Substance abuse or dependence
Current depressive episode with clear suicidal plans or suicidal behavior
Trial design
Treatments tested in this trial
- Fluoxetine
- Sertraline
- Vortioxetine
- Duloxetine
- Aripiprazole
- Lithium Carbonate
- Olanzapine
- GCBT
Treatment groups
8
Treatment groupsSee each treatment group below.
Sponsors and collaborators
First Affiliated Hospital of Chongqing Medical University
Lead sponsor
The Second Affiliated Hospital of Chongqing Medical University
Collaborator
Second Xiangya Hospital of Central South University
Collaborator
Children's Hospital of Chongqing Medical University
Collaborator