Skip to content

Effect of aripiprazole combined with antidepressants on cognitive function of patients with depressive disorder and clinical efficacy evaluation

Effect of aripiprazole combined with antidepressants on cognitive function of patients with depressive disorder and clinical efficacy evaluation

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900028541
Enrollment
Unknown
Registered
2019-12-27
Start date
2020-01-01
Completion date
Unknown
Last updated
2020-01-06

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

Conditions

Major Depressive Disorder

Interventions

Control Group:Treat with the escitalopram
Experimental group:Treat with aripiprazole and escitalopram

Sponsors

Shandong Mental Health Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1. Meet the diagnostic criteria for DSM-5 'major depressive disorder'; 2. Patients with first episode of major depressive disorder who have not received any treatment, or have not received any treatment in the last 2 months; 3. Han nationality, 18-45 years old, regardless of gender; 4. Aged of first onset >=18 years; 5. Hamilton Depression Scale (HAMD-17) >=17, mood disorder questionnaire (MDQ) <7; 6. Junior high school or above; 7. Participate in this study voluntarily and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. A history of serious physical diseases, organic brain diseases and craniocerebral trauma; 2. Patients with psychotic symptoms or other mental disorders; 3. Serious suicide and nssi risk and behavior; 4. No cooperation or inability to effectively complete the experimenter in the research process; 5. Persons known to be allergic to the ingredients of research drugs; 6. Family history of bipolar disorder; 7. Those who are currently in the perinatal period or have a pregnancy plan; 8. Patients who intend to receive MECT during treatment.

Design outcomes

Primary

MeasureTime frame
Serum prolactin levels;Hamilton Depression Scale;Hamilton Anxiety Scale;Mood Disorder Questionnaire;Thinc-it;Wsiconsin Card Sorting Test;Continuous Perfomance Test;Rating Scale for extrapyramidal Side Effects;Liver function;Blood glucose;Blood lipids;

Countries

China

Contacts

Public ContactGuanglei XUN

Shandong Mental Health Center

xungl@163.com+86 15069053599

Outcome results

None listed

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