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Terminated Phase 2 Interventional

A 2 Week Blinded Study For Pain Due To Arthritis Of The Knee

ClinicalTrials.gov ID: NCT00483977

Public ClinicalTrials.gov record NCT00483977. 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 26, 2026, 10:37 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 2 Week, Randomized, Double Blind, Placebo And Positive Controlled, Parallel Group, Multicentre Study To Assess The Efficacy And Tolerability Of PF-00592379 In Patients With Moderate To Severe Pain Due To Osteoarthritis

Brief summary

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

The primary aim is to assess if PF-00592379 is able to reduce pain in patients with osteoarthritis of the knee.

Study identification

NCT ID
NCT00483977
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Pfizer
Industry
Enrollment
113 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 75 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
Jun 2007 (Type not available)
Primary completion
Dec 2007 (Actual)
Completion
Dec 2007 (Actual)
Last update posted
Apr 29, 2011

2007

United States locations

U.S. sites
21
U.S. states
11
U.S. cities
20
Facility City State ZIP Site status
Pfizer Investigational Site Mobile Alabama 36608 —
Pfizer Investigational Site Tucson Arizona 85741 —
Pfizer Investigational Site Carmichael California 95608 —
Pfizer Investigational Site Fair Oaks California 95628 —
Pfizer Investigational Site Orangevale California 95662 —
Pfizer Investigational Site Roseville California 95661 —
Pfizer Investigational Site Sacramento California 95825 —
Pfizer Investigational Site Boca Raton Florida 33486 —
Pfizer Investigational Site DeLand Florida 32720 —
Pfizer Investigational Site Hollywood Florida 33021 —
Pfizer Investigational Site Longwood Florida 32779 —
Pfizer Investigational Site Miami Florida 33186 —
Pfizer Investigational Site Louisville Kentucky 40213 —
Pfizer Investigational Site Madisonville Kentucky 42431 —
Pfizer Investigational Site St Louis Missouri 63141 —
Pfizer Investigational Site Las Vegas Nevada 89146 —
Pfizer Investigational Site New York New York 10022-1009 —
Pfizer Investigational Site Durham North Carolina 27704 —
Pfizer Investigational Site Cincinnati Ohio 45227 —
Pfizer Investigational Site Cincinnati Ohio 45242 —
Pfizer Investigational Site Richmond Virginia 23294 —

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 NCT00483977, 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 Apr 29, 2011 · Synced Oct 26, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00483977 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →