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Terminated Phase 4 Interventional Results available

28-30 Month Study Comparing Paliperidone Palmitate With Oral Risperidone for Treating Adults Diagnosed With Schizophrenia Within the Past 5 Years

ClinicalTrials.gov ID: NCT00946985

Public ClinicalTrials.gov record NCT00946985. 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 1, 2026, 7:45 PM 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 Prospective, Randomized, Active-controlled, Rater-blinded Study of the Prevention of Relapse Comparing Paliperidone Palmitate With Oral Risperidone in Adults With Recently-Diagnosed Schizophrenia Who Are at High Risk of Relapse

Brief summary

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

The study will assess the use of paliperidone palmitate compared with oral risperidone in delaying time to relapse in patients recently diagnosed with schizophrenia who are at high risk of relapse.

Study identification

NCT ID
NCT00946985
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 4
Enrollment
163 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 35 Years
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
May 31, 2009
Primary completion
Feb 28, 2010
Completion
Feb 28, 2010
Last update posted
Sep 9, 2012

2009 – 2010

United States locations

U.S. sites
23
U.S. states
16
U.S. cities
23
Facility City State ZIP Site status
Not listed Little Rock Arkansas
Not listed Garden Grove California
Not listed San Diego California
Not listed Washington D.C. District of Columbia
Not listed Kissimmee Florida
Not listed Tampa Florida
Not listed Chicago Illinois
Not listed Hoffman Estates Illinois
Not listed Kingsport Indiana
Not listed Lake Charles Louisiana
Not listed Shreveport Louisiana
Not listed Pittsfield Massachusetts
Not listed Minneapolis Minnesota
Not listed Flowood Mississippi
Not listed Creve Coeur Missouri
Not listed St Louis Missouri
Not listed Omaha Nebraska
Not listed Brooklyn New York
Not listed Middleburg Heights Ohio
Not listed Arlington Texas
Not listed Austin Texas
Not listed Irving Texas
Not listed Portsmount Virginia

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 49 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00946985, 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 Sep 9, 2012 · Synced Sep 1, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00946985 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →