Patient-Reported Outcomes in the Treatment of Schizophrenia
This study has been completed.
Sponsor:
Solvay Pharmaceuticals
Information provided by:
Solvay Pharmaceuticals
ClinicalTrials.gov Identifier:
NCT00230828
First received: September 12, 2005
Last updated: September 6, 2007
Last verified: September 2007
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Purpose
Patient-reported health economic outcomes for patients enrolled in S1543003 and S1543004 protocols
| Condition | Intervention | Phase |
|---|---|---|
|
Schizophrenia |
Drug: bifeprunox |
Phase 3 |
| Study Type: | Interventional |
| Study Design: | Allocation: Non-Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Double-Blind Primary Purpose: Treatment |
| Official Title: | Patient-Reported Outcomes With Bifeprunox or Olanzapine in the Treatment of Schizophrenia. A Pharmacoeconomic Study Carried Out in Connection With the S1543003 And S1543004 Clinical Trials |
Resource links provided by NLM:
Further study details as provided by Solvay Pharmaceuticals:
Eligibility| Ages Eligible for Study: | 18 Years to 75 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Participate in S1543003 and S1543004 in the U.S. sites
Exclusion Criteria:
- Participate in S1543003 and S1543004 other than U.S. sites
Contacts and Locations
More Information
No publications provided
| ClinicalTrials.gov Identifier: | NCT00230828 History of Changes |
| Other Study ID Numbers: | S154.3.005 |
| Study First Received: | September 12, 2005 |
| Last Updated: | September 6, 2007 |
| Health Authority: | United States: Food and Drug Administration |
Additional relevant MeSH terms:
|
Schizophrenia Schizophrenia and Disorders with Psychotic Features Mental Disorders |
ClinicalTrials.gov processed this record on May 22, 2013