Patient-reported Outcomes in the Treatment of Schizophrenia

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE3

Study Classification

INTERVENTIONAL

Study Start Date

2005-05-31

Brief Summary

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Patient-reported health economic outcomes for patients enrolled in S1543003 and S1543004 protocols

Detailed Description

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Conditions

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Schizophrenia

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Interventions

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bifeprunox

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Participate in S1543003 and S1543004 in the U.S. sites

Exclusion Criteria

* Participate in S1543003 and S1543004 other than U.S. sites

Minimum Eligible Age

18 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Principal Investigators

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Global Clinical Director Solvay

Role: STUDY_DIRECTOR

Solvay Pharmaceuticals

Other Identifiers

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S154.3.005

Identifier Type: -

Identifier Source: org_study_id