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Completed Phase 3 Interventional Results available

Study of an Investigational Drug for the Prevention of Thrombosis-related Events Following Hip Replacement Surgery (ADVANCE-3)

ClinicalTrials.gov ID: NCT00423319

Public ClinicalTrials.gov record NCT00423319. 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 Sep 2, 2026, 9:17 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 Phase 3 Randomized, Double-blind, Active-controlled, Parallel-group, Multi-center Study to Evaluate the Safety and Efficacy of Apixaban in Subjects Undergoing Elective Total Hip Replacement Surgery (The Advance-3 Study Apixaban Dosed Orally Versus Anticoagulation With Injectable Enoxaparin to Prevent Venous Thromboembolism)

Brief summary

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

The purpose of this study is to learn whether apixaban can prevent the blood clots in the leg (deep vein thrombosis) and lung (pulmonary embolism) that sometimes occur after hip replacement surgery and to learn how apixaban compares with enoxaparin in preventing these clots. The safety of apixaban will also be studied

Study identification

NCT ID
NCT00423319
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Bristol-Myers Squibb
Industry
Enrollment
5,407 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 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
Feb 28, 2007
Primary completion
Aug 31, 2009
Completion
Aug 31, 2009
Last update posted
May 13, 2014

2007 – 2009

United States locations

U.S. sites
19
U.S. states
9
U.S. cities
15
Facility City State ZIP Site status
Capstone Clinical Trials, Inc Birmingham Alabama 35209
West Alabama Research, Llc Birmingham Alabama 35209
Martin Bowen Hefley Orthopedics Little Rock Arkansas 72205
Orthoarkansas, P.A. Little Rock Arkansas 72205
Uc Davis Medical Center Sacramento California 95817
Colorado Orthopedic Consultants, Pc Aurora Colorado 80012
Advanced Orthopedic And Sports Medicine Specilists Denver Colorado 80230
Denver-Vail Orthopedics, P.C. Denver Colorado 80230
Pab Clinical Research Brandon Florida 33511
Research Alliance, Inc. Clearwater Florida 33756
Shrock Orthopedic Research Fort Lauderdale Florida 33316
Phoenix Clinical Research, Llc Tamarac Florida 33321
Atlanta Knee And Sports Medicine Decatur Georgia 30033
Americana Orthopedics Boise Idaho 83702
Bosie Orthopedic Clinic Meridian Idaho 83642
University Orthopedic Center Altoona Pennsylvania 16602
Gill Orthopedic Center Lubbock Texas 79410
Robert R. King, Md Lubbock Texas 79410
Unlimited Research San Antonio Texas 78217

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 124 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00423319, 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 May 13, 2014 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00423319 live on ClinicalTrials.gov.

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