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Completed Phase 4 Interventional Results available

Study to Measure Drug Satisfaction of Patients With Schizophrenia After Switching From Risperidone to Paliperidone

ClinicalTrials.gov ID: NCT00535132

Public ClinicalTrials.gov record NCT00535132. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 2, 2026, 1:55 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Blinded-initiation Study of Medication Satisfaction in Subjects With Schizophrenia Treated With Paliperidone ER After Suboptimal Response to Oral Risperidone

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to evaluate medication satisfaction after at least 4 weeks of paliperidone ER (extended-release), an antipsychotic, treatment in patients with schizophrenia who were previously taking either 4 or 6 mg of risperidone daily by mouth, but who are not satisfied with their treatment.

Study identification

NCT ID
NCT00535132
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Enrollment
201 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 30, 2007
Primary completion
Jun 30, 2008
Completion
Jun 30, 2008
Last update posted
May 8, 2014

2007 – 2008

United States locations

U.S. sites
15
U.S. states
8
U.S. cities
15
Facility City State ZIP Site status
Not listed Cerritos California
Not listed Garden Grove California
Not listed Huntington Beach California
Not listed Pico Rivera California
Not listed San Diego California
Not listed Santa Ana California
Not listed Torrance California
Not listed Atlanta Georgia
Not listed Chicago Illinois
Not listed Flowood Mississippi
Not listed Clementon New Jersey
Not listed Brooklyn New York
Not listed Philadelphia Pennsylvania
Not listed Austin Texas
Not listed Irving Texas

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 25 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00535132, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted May 8, 2014 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00535132 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →