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Completed Phase 3 Interventional Results available

Efficacy And Safety Of Pregabalin For Pain Following Total Knee Replacement

ClinicalTrials.gov ID: NCT00442546

Public ClinicalTrials.gov record NCT00442546. 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 Apr 22, 2026, 11:53 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 Multicenter, Double-Blind Randomized, Placebo-Controlled Study Of The Efficacy And Safety Of Pregabalin In The Treatment Of Subjects With Post-Operative Pain Following Total Knee Arthroplasty (TKA)

Study identification

NCT ID
NCT00442546
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Pfizer's Upjohn has merged with Mylan to form Viatris Inc.
Industry
Enrollment
307 participants

Conditions and interventions

Interventions

  • Placebo Drug
  • pregabalin Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 80 Years
Sex
All
Healthy volunteers
Not listed

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Apr 30, 2007
Primary completion
Nov 30, 2008
Completion
Nov 30, 2008
Last update posted
Jan 21, 2021

2007 – 2008

United States locations

U.S. sites
27
U.S. states
13
U.S. cities
24
Facility City State ZIP Site status
Pfizer Investigational Site Northport Alabama 35476
Pfizer Investigational Site Tuscaloosa Alabama 35401
Pfizer Investigational Site Tuscaloosa Alabama 35406
Pfizer Investigational Site Phoenix Arizona 85023
Pfizer Investigational Site Little Rock Arkansas 72205
Pfizer Investigational Site Miami Florida 331036
Pfizer Investigational Site Vero Beach Florida 32960
Pfizer Investigational Site Chicago Illinois 60612
Pfizer Investigational Site Galesburg Illinois 61401
Pfizer Investigational Site Lafayette Louisiana 70503
Pfizer Investigational Site New Iberia Louisiana 70563
Pfizer Investigational Site Baltimore Maryland 21218
Pfizer Investigational Site Egg Harbor New Jersey 08234
Pfizer Investigational Site Pomona New Jersey 08205
Pfizer Investigational Site Voorhees Township New Jersey 08043
Pfizer Investigational Site New York New York 10021
Pfizer Investigational Site Charlotte North Carolina 28207
Pfizer Investigational Site Columbus Ohio 43214
Pfizer Investigational Site Columbus Ohio 43215
Pfizer Investigational Site Upper Arlington Ohio 43220
Pfizer Investigational Site Allentown Pennsylvania 18103
Pfizer Investigational Site King of Prussia Pennsylvania 19406
Pfizer Investigational Site Philadelphia Pennsylvania 19107
Pfizer Investigational Site Pittsburgh Pennsylvania 15213-2582
Pfizer Investigational Site Pittsburgh Pennsylvania 15232
Pfizer Investigational Site Dallas Texas 75390
Pfizer Investigational Site Houston Texas 77030

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 NCT00442546, 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 Jan 21, 2021 · Synced Apr 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00442546 live on ClinicalTrials.gov.

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