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Completed Phase 3 Interventional

Efficacy Study Exploring the Effects on Cognition of Sertindole Versus Comparator in Patients With Schizophrenia

ClinicalTrials.gov ID: NCT00654706

Public ClinicalTrials.gov record NCT00654706. 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 Oct 27, 2026, 6:22 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 Randomised, Double-Blind, Parallel-Group, Flexible-Dose Study Exploring the Neurocognitive Effect of Sertindole Versus Comparator in Patients With Schizophrenia Using the MATRICS Consensus Cognitive Battery (MCCB)

Brief summary

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

The objective of this study is to explore the neurocognitive efficacy of Sertindole versus comparator in patients with schizophrenia using the MCCB.

Study identification

NCT ID
NCT00654706
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
H. Lundbeck A/S
Industry
Enrollment
264 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 55 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
Mar 2008 (Type not available)
Primary completion
Jan 2010 (Actual)
Completion
Mar 2010 (Actual)
Last update posted
May 28, 2014

2008 – 2010

United States locations

U.S. sites
26
U.S. states
12
U.S. cities
26
Facility City State ZIP Site status
US017 Garden Grove California 92845 —
US008 National City California 91950 —
US001 Pasadena California 91107 —
US006 Pico Rivera California 90660 —
US011 San Diego California 92126 —
US014 Stanford California 94305 —
US026 Torrance California 90502 —
US016 Aurora Colorado 80045 —
US015 Orange City Florida 32763 —
US010 Tampa Florida 33613 —
US007 Atlanta Georgia 30308 —
US024 Chicago Illinois 60640 —
US002 Joliet Illinois 60435 —
US012 Baltimore Maryland 21204 —
US027 Glen Burnie Maryland 21061 —
US019 Lebanon New Hampshire 03756 —
US021 Clementon New Jersey 08021 —
US013 Brooklyn New York 11203 —
US025 Staten Island New York 10305 —
US005 Charlotte North Carolina 28211 —
US018 Durham North Carolina 27705 —
US022 Philadelphia Pennsylvania 19139 —
US023 Austin Texas 78754 —
US020 Dallas Texas 75235 —
US004 DeSoto Texas 75115 —
US028 Houston Texas 77008 —

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00654706, 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 28, 2014 · Synced Oct 27, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00654706 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →