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Completed Phase 2 Interventional Results available

Odiparcil For The Prevention Of Venous Thromboembolism

ClinicalTrials.gov ID: NCT00244725

Public ClinicalTrials.gov record NCT00244725. 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, 4:52 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 Dose Ranging Trial for the Evaluation of the Safety, Tolerability and Efficacy of Odiparcil in the Prevention of Venous Thromboembolism Following Total Knee Replacement Surgery

Brief summary

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

Odiparcil is being studied to determine if it can prevent blood clots from forming after a total knee replacement and also to prove that odiparcil is safe.

Study identification

NCT ID
NCT00244725
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
961 participants

Conditions and interventions

Eligibility (public fields only)

Age range
35 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
Sep 2005 (Type not available)
Primary completion
Sep 2006 (Actual)
Completion
Sep 2006 (Actual)
Last update posted
May 2, 2017

2005 – 2006

United States locations

U.S. sites
46
U.S. states
20
U.S. cities
40
Facility City State ZIP Site status
GSK Investigational Site Birmingham Alabama 35209 —
GSK Investigational Site Mobile Alabama 36608 —
GSK Investigational Site Phoenix Arizona 85023 —
GSK Investigational Site Little Rock Arkansas 72205 —
GSK Investigational Site Banning California 92220 —
GSK Investigational Site Sacramento California 95817 —
GSK Investigational Site Torrance California 90509 —
GSK Investigational Site Yuba City California 95991 —
GSK Investigational Site Colorado Springs Colorado 80907 —
GSK Investigational Site Lonetree Colorado 80124 —
GSK Investigational Site Clearwater Florida 33756 —
GSK Investigational Site DeLand Florida 32720 —
GSK Investigational Site Jacksonville Florida 32216 —
GSK Investigational Site Sarasota Florida 34239 —
GSK Investigational Site Sarsota Florida 34239 —
GSK Investigational Site St. Petersburg Florida 33701 —
GSK Investigational Site Decatur Georgia 30033 —
GSK Investigational Site Boise Idaho 83702 —
GSK Investigational Site Lexington Kentucky 40509 —
GSK Investigational Site Baton Rouge Louisiana 70808 —
GSK Investigational Site Baltimore Maryland 21209 —
GSK Investigational Site Baltimore Maryland 21215-5271 —
GSK Investigational Site Baltimore Maryland 21218 —
GSK Investigational Site Warren Michigan 48089 —
GSK Investigational Site Mineola New York 11501 —
GSK Investigational Site Charlotte North Carolina 28207 —
GSK Investigational Site Durham North Carolina 27704 —
GSK Investigational Site Cincinnati Ohio 45242 —
GSK Investigational Site Cleveland Ohio 44195 —
GSK Investigational Site Toledo Ohio 43614 —
GSK Investigational Site Allentown Pennsylvania 18103 —
GSK Investigational Site Altoona Pennsylvania 16601 —
GSK Investigational Site Camp Hill Pennsylvania 17011 —
GSK Investigational Site Hershey Pennsylvania 17033 —
GSK Investigational Site Philadelphia Pennsylvania 19107 —
GSK Investigational Site Philadelphia Pennsylvania 19140 —
GSK Investigational Site Dallas Texas 75231 —
GSK Investigational Site Dallas Texas 75246 —
GSK Investigational Site Lubbock Texas 79410 —
GSK Investigational Site San Antonio Texas 78217 —
GSK Investigational Site San Antonio Texas 78229 —
GSK Investigational Site Norfolk Virginia 23507 —
GSK Investigational Site Richmond Virginia 23229 —
GSK Investigational Site Richmond Virginia 23249 —
GSK Investigational Site Huntington West Virginia 25701 —
GSK Investigational Site Marshfield Wisconsin 54449 —

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 55 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00244725, 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 2, 2017 · 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 NCT00244725 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →