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Pharmacogenomic study of schizophrenia

The genome-wide association and pharmacogenomic study of schizophrenia

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-10000934
Enrollment
Unknown
Registered
2010-07-06
Start date
2010-05-01
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

1:Perphenazine 16-64 mg/d (N=250) or Haloperidol 6-20 mg/d (N=250)
2:Risperidone 2-6mg/d
3:Olanzapine 5-20 mg/d
4:Quetiapine 400-750mg/d
5:Aripiperazole 10~30 mg/d
6:Ziprasidone 80-160 mg/d

Sponsors

The Sixth Hospital / Institute of Mental Health, Peking University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1. Both the patients and their parents are Chinese Han descents; 2. The schizophrenia patients at first-onset or the chronic patients with acute and severe symptoms; 3. The total scores of the PANSS are more than 70; 4. All of the subjects give the written informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with pregnancy or breast-feeding; 2. Patients with the contraindications of the recommended drugs; 3. Patients with severe or unstable physical diseases; 4. Patients with following heart diseases: QTc>450 ms in male, or QTc>470ms in female; Decompensated and congestive heart failure; Complete left bundle branch block delay.

Design outcomes

Primary

MeasureTime frame
Reduction rate of PANSS total score;

Countries

China

Contacts

Public ContactDai Zhang
daizhang@bjmu.edu.cn+86 010 82801937

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 23, 2026