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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 Jul 23, 2026, 10:09 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

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

  • Oxycodone Drug
  • Placebo Drug
  • PF-000592379 Drug

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
May 31, 2007
Primary completion
Nov 30, 2007
Completion
Nov 30, 2007
Last update posted
Apr 28, 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 28, 2011 · Synced Jul 23, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00483977 live on ClinicalTrials.gov.

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