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The study on clinical and biological characters of bipolar depression and the treatment scheme optimizing

The study on clinical and biological characters of bipolar depression and the treatment scheme optimizing

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-TNRC-10001112
Enrollment
Unknown
Registered
2010-11-23
Start date
2007-09-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

bipolar depressive disorder

Interventions

20:Lithium, Sodium valproate, Lamotrigine, MECT, Sertraline, Citalopram, Escitalopram, venlafaxine, Quetiapine, Olanzapine, Risperidone, sulpiride

Sponsors

Guangzhou Scientific and Technological Bureau, Guangzhou Board of Health
Lead Sponsor

Eligibility

Sex/Gender
All
Age
17 Years to 65 Years

Inclusion criteria

Inclusion criteria: Include the outpatients and inpatients met DSM-IV-TR bipolar depressive disorder and major depressive disorder; age of 17~65, both male and femal; Hamilton Depression Scale 17 item >=18; sign the informed consent.

Exclusion criteria

Exclusion criteria: Exclude the patients combinating with severe physical conditions and endocrinopathy; nonselective monamine oxidase inhibitors were used 1 month before included; long-term antipsychotics were used 2 month before included; thyroxine was used 3 month before included, and hornone was using when included; pregnant and lactating women, and who didn't take effective practise contraception.

Design outcomes

Primary

MeasureTime frame
Manic/hypomanic episode;General effects of CGI;

Secondary

MeasureTime frame
HAMA deduction rate;BPRS deduction rate;

Countries

China

Contacts

Public ContactXu Guiyun
13650774898@163.com+86 13650774898

Outcome results

None listed

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