Evaluation Of Fondaparinux (Also Called ARIXTRA) 2.5 mg Subcutaneously Once Daily For The Treatment Of Superficial Thrombophlebitis (Also Known As Superficial Vein Thrombosis) - Trial NCT00443053
Access comprehensive clinical trial information for NCT00443053 through Pure Global AI's free database. This Phase 3 trial is sponsored by GlaxoSmithKline and is currently Completed. The study focuses on Thrombosis, Venous. Target enrollment is 3002 participants.
This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.
Study Focus
Sponsor & Location
GlaxoSmithKline
Timeline & Enrollment
Phase 3
Mar 01, 2007
Jul 01, 2009
Primary Outcome
Number of Participants With at Least on Event of Venous Thromboembolism (VTE) and/or Death From Any Cause Recorded up to Day 47
Summary
To evaluate fondaparinux 2.5mg subcutaneously once daily for 45 days in the treatment of
 acute (recent) superficial thrombophlebitis.
ICD-10 Classifications
Data Source
ClinicalTrials.gov
NCT00443053
Non-Device Trial

