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| Sponsored by: |
Department of Veterans Affairs |
| Information provided by: | Department of Veterans Affairs |
| ClinicalTrials.gov Identifier: | NCT00018642 |
Purpose
The purpose of this research study is to determine whether a new drug for schizophrenia is better for the maintenance treatment than a standard drugs currently prescribed. The new medication is called quetiapine and it will be compared with a standard medication called haloperidol decanoate. The study will determine if quetiapine causes fewer problems than haloperidol with side effects such as stiffness and restlessness and whether it costs the VA more or less to treat patients with quetiapine. In addition, blood samples will be collected every three months to determine if certain chemicals in the blood can influence the outcome of the subjects' illness.
| Condition | Intervention |
|
Schizophrenia Schizoaffective Disorder |
Drug: quetiapine Drug: haloperidol decanoate |
| MedlinePlus related topics: | Schizophrenia |
| Drug Information available for: | Quetiapine Quetiapine fumarate Haloperidol Haloperidol decanoate |
| Study Type: | Interventional |
| Study Design: | Treatment, Randomized, Uncontrolled, Parallel Assignment, Efficacy Study |
| Official Title: | Predicting the Optimal Pharmacotherapy for Outpatients With Schizophrenia |
Eligibility
| Ages Eligible for Study: | 18 Years to 60 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria
Exclusion Criteria
Contacts and Locations
More Information
| Study ID Numbers: | MHBS-042-96F |
| First Received: | July 3, 2001 |
| Last Updated: | June 23, 2005 |
| ClinicalTrials.gov Identifier: | NCT00018642 |
| Health Authority: | United States: Federal Government |
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