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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01668810
Other study ID # RISSCH4255
Secondary ID
Status Recruiting
Phase N/A
First received August 16, 2012
Last updated August 17, 2012
Start date July 2012
Est. completion date July 2013

Study information

Verified date July 2012
Source Peking University
Contact Yun-Ai Su, Phd.
Phone 8610-82801960
Email suyunai@gmail.com
Is FDA regulated No
Health authority China: Food and Drug Administration
Study type Observational

Clinical Trial Summary

The investigators aimed to examine the psychotropic prescription pattern in China.


Recruitment information / eligibility

Status Recruiting
Enrollment 7000
Est. completion date July 2013
Est. primary completion date September 2012
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: aged 18-65, inpatient or outpatient, Patient must be willing and able to give written informed consent,the patient suffers from schizophrenia or depression or bipolar disorder -

Exclusion Criteria:aged<18or aged>65

Study Design

Observational Model: Ecologic or Community, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
China Institute of mental health, Peking University Beijing Beijing

Sponsors (2)

Lead Sponsor Collaborator
Peking University Xian-Janssen Pharmaceutical Ltd.

Country where clinical trial is conducted

China, 

See also
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Completed NCT04919889 - Implementation and Effectiveness of a Community-based Exercise on Prescription Program for Adults With Chronic Diseases
Active, not recruiting NCT06212895 - Expectations of Patients Regarding Exercise in an Outpatient Clinic