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The genetic association study on individual difference of therapeutic effects of antipsychotic medication

The personalized therapy of major depression disorders and schizophrenia -- the application of the techology of molecular classification

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-RNC-09000521
Enrollment
Unknown
Registered
2009-08-18
Start date
2008-05-01
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

schizophrenia

Interventions

Qutiapine 400-750mg/d
Clozapine 200-600 mg/d
Perphenazine 20-60 mg/d

Sponsors

Sixth Hospital, Peking University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Male or female, 18-60 years old; 2. Chinese of Han descents; 3. with written informed consent for genetic study; 4. recruited from the outpatient and inpatient departments of psychiatric hospitals; 5. fulfilling the DSM-IV criteria for schizophrenia; 6. The total score of the PANSS of patients were above 60 when they are enrolled in the study.

Exclusion criteria

Exclusion criteria: The patients will be excluded when they: 1. be diagnosed as the mental retardation, alcohol or drug addiction, according to the DSM-IV; 2. suffered from the severe physical diseases, such as diabetes mellitus, thyroid gland disease, hypertension, other diseases as angel-closure glaucoma, epilapsy (febrile convulsion could be included); 3. ever received the sustained-release antipsychotics, ECT or clozapine therapy one month ago; 4. ever suffered from severe side effects related to antipsychotics, such as NMS, EPS, TD; 5. with severe suicidal ideas or obvious excitation and agitation; 6. with obvious abnormal index of laboratory examination; 7. with poor therapeutic compliance or without custodians; 8. with QTc interphase longer than 470 mses; 9. female in pregnancy or lactation periods or planning to pregnancy.

Design outcomes

Primary

MeasureTime frame
Positive and negative symptom scale (PANSS);

Countries

China

Contacts

Public ContactZHang Dai
daizhang@bjmu.edu.cn+86 010 82801937

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 11, 2026