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CompletedNCT00202007

Efficacy and Safety Study of Aripiprazole to Treat Schizophrenia

Medication studyAges 18–65China
The study in practice

Understand this study

Who was this study for?

This study was for people with schizophrenia. Listed age limits: 18 years to 65 years. Other eligibility criteria applied.

Listed locations
Guangzhou, China · Wuhan, China and 3 more locationsSee all locations and recruitment
Activities
Medication described in the protocol
Compensation
Payment and expense reimbursement have not been verified.
Study clarity

Study information

Study start dateFebruary 2005
Recruitment status
Completed
Enrollment listed in the registry
240
Sponsor
Otsuka Beijing Research Institute
Sponsor type
Research institute
Study type
Drug
Intervention type
Medication / drug
Study phase
Phase 2Usually explores whether the intervention may work, while continuing to monitor safety.
Locations
China
Age range
From 18 Years to 65 Years
Official registry ID
NCT00202007
Official title
Show the full official title

A Multi-Center, Randomized, Double-Blind Study, Comparing With Risperidone, to Evaluate the Efficacy and Safety of Aripiprazole in the Treatment of Patients With Schizophrenia

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Recruitment & locations

Completed

Guangzhou · Wuhan · Nanjing

2 more locations
  • Beijing
  • Shanghai
FAQ

Questions about this study

Who is behind this study?

The study sponsor is Otsuka Beijing Research Institute, a research institute.

Did this study involve medication?

Yes. The study involved medication, including Aripiprazole tablet, 5-30mg/day, oral, 6 weeks and Risperidone tablet, 1-6mg/day, oral, 6 weeks.

Who was this study for?

This study was for people with schizophrenia. Listed age limits: 18 years to 65 years. Other eligibility criteria applied.

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