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Terminated Phase 3 Interventional

Treatment of Elderly Subjects With Psychosis and Behavioral Disturbances Associated With Dementia of the Alzheimer's Type

ClinicalTrials.gov ID: NCT00160147

Public ClinicalTrials.gov record NCT00160147. 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 Jul 23, 2026, 12:12 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 Randomized, Double-Blind, Placebo-controlled, Efficacy, Safety, and Tolerability Study of Bifeprunox in the Treatment of Elderly Subjects With Psychosis and Behavioral Disturbances Associated With Dementia of the Alzheimer's Type

Study identification

NCT ID
NCT00160147
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Solvay Pharmaceuticals
Industry
Enrollment
60 participants

Conditions and interventions

Interventions

  • bifeprunox Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
65 Years to 90 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
Nov 30, 2005
Primary completion
Dec 31, 2007
Completion
Dec 31, 2007
Last update posted
Feb 8, 2015

2005 – 2008

United States locations

U.S. sites
35
U.S. states
17
U.S. cities
31
Facility City State ZIP Site status
Site 912 Phoenix Arizona
Site 902 Carson California
Site 903 Long Beach California
Site 911 Pasadena California
Site 922 San Marino California
Site 910 Santa Ana California
Site 929 Hamden Connecticut
Site 914 New Britain Connecticut
Site 931 Norwalk Connecticut
Site 901 Miami Florida
Site 907 North Miami Florida
Site 933 Orange City Florida
Site 934 Atlanta Georgia
Site 917 Blue Ridge Georgia
Site 925 Newnan Georgia
Site 904 New Orleans Louisiana
Site 905 Shreveport Louisiana
Site 906 Shreveport Louisiana
Site 919 Bedford Massachusetts
Site 923 Boston Massachusetts
Site 942 Flowood Mississippi
Site 927 St Louis Missouri
Site 930 St Louis Missouri
Site 940 St Louis Missouri
Site 941 Olean New York
Site 921 Staten Island New York
Site 909 Cincinnati Ohio
Site 908 Oklahoma City Oklahoma
Site 916 Oklahoma City Oklahoma
Site 935 Philadelphia Pennsylvania
Site 932 Humboldt Tennessee
Site 936 Austin Texas
Site 928 Dallas Texas
Site 913 Williamsburg Virginia
Site 918 Waukesha Wisconsin

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 16 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00160147, 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 Feb 8, 2015 · Synced Jul 23, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00160147 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →