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Completed Phase 3 Interventional

Depression Study In Elderly Patients

ClinicalTrials.gov ID: NCT00067444

Public ClinicalTrials.gov record NCT00067444. 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 Nov 5, 2026, 1:16 AM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Fixed Dose Study Evaluating the Efficacy and Safety of Paroxetine CR in Elderly Outpatients Diagnosed With Major Depressive Disorder

Brief summary

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

Major Depressive Disorder (MDD) Study in Elderly Outpatients

Study identification

NCT ID
NCT00067444
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
560 participants

Conditions and interventions

Eligibility (public fields only)

Age range
60 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
Jun 2003 (Type not available)
Primary completion
Jan 2005 (Actual)
Completion
Jan 2005 (Actual)
Last update posted
Sep 1, 2016

2003 – 2005

United States locations

U.S. sites
46
U.S. states
23
U.S. cities
43
Facility City State ZIP Site status
GSK Investigational Site Little Rock Arkansas 72223 —
GSK Investigational Site Anaheim California 92805 —
GSK Investigational Site Beverly Hills California 90210 —
GSK Investigational Site El Centro California 92243 —
GSK Investigational Site Los Angeles California 90048 —
GSK Investigational Site Redlands California 92374 —
GSK Investigational Site Santa Ana California 92705 —
GSK Investigational Site Colorado Springs Colorado 80904 —
GSK Investigational Site Norwich Connecticut 06360 —
GSK Investigational Site Jacksonville Florida 32216 —
GSK Investigational Site Leesburg Florida 34748 —
GSK Investigational Site Miami Florida 33125 —
GSK Investigational Site Miami Florida 33156 —
GSK Investigational Site Orlando Florida 32806 —
GSK Investigational Site Sebring Florida 33870 —
GSK Investigational Site St. Petersburg Florida 33710 —
GSK Investigational Site West Palm Beach Florida 33407 —
GSK Investigational Site Marietta Georgia 30060 —
GSK Investigational Site Boise Idaho 83704 —
GSK Investigational Site Lafayette Indiana 47905 —
GSK Investigational Site Overland Park Kansas 66211 —
GSK Investigational Site Prairie Village Kansas 66206 —
GSK Investigational Site Gaithersburg Maryland 20877 —
GSK Investigational Site Rockville Maryland 20852 —
GSK Investigational Site Braintree Massachusetts 02184 —
GSK Investigational Site Nashua New Hampshire 03060 —
GSK Investigational Site Clementon New Jersey 08021 —
GSK Investigational Site Princeton New Jersey 08540 —
GSK Investigational Site Mount Kisco New York 10549 —
GSK Investigational Site New York New York 10021 —
GSK Investigational Site New York New York 10024 —
GSK Investigational Site Charlotte North Carolina 28209 —
GSK Investigational Site Greensboro North Carolina 27401 —
GSK Investigational Site Raleigh North Carolina 27609 —
GSK Investigational Site Oklahoma City Oklahoma 73118 —
GSK Investigational Site Eugene Oregon 97401 —
GSK Investigational Site Conshohocken Pennsylvania 19428 —
GSK Investigational Site Philadelphia Pennsylvania 19104 —
GSK Investigational Site Philadelphia Pennsylvania 19115 —
GSK Investigational Site East Providence Rhode Island 02914 —
GSK Investigational Site Charleston South Carolina 29407 —
GSK Investigational Site Memphis Tennessee 38119 —
GSK Investigational Site Austin Texas 78756 —
GSK Investigational Site Houston Texas 77007 —
GSK Investigational Site San Antonio Texas 78229-3815 —
GSK Investigational Site Salt Lake City Utah 84107 —

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 NCT00067444, 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 1, 2016 · Synced Nov 5, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00067444 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →