drugset / Trial / NCT00311896

Efficacy & Safety of Prophylaxis With Bemiparin in Cancer Patients With a Central Venous Catheter (BECAT)

NCT00311896

RandomizedParallel-groupDouble-blindPrevention

Summary

The purpose of this study is to evaluate the efficacy and safety of the subcutaneous administration for 45 days of Bemiparin (3,500 UI/day) in cancer patients with a CVC, to prevent CVC-related deep venous thrombosis (CVC-DVT)

Timeline

Start
2005-07
Primary completion
2009-02
Completion
2010-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Bemiparin Other / unclassified 3500 iu Subcutaneous