This is a Phase III open-labed, multicenter, prospective, randomised study, and comparative 3-arms of 140 patients (i.e. 420 total patients). Study period (date of first inclusion/last inclusion): 3 years Treatment period : 3 months
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Enrollment
420
Oncologie Médicale
Limoges, France
Evaluation of the prevalence of symptomatic or asymptomatic deep venous thrombosis in cancer patients with implantable device for central venous access with or without prophylaxis :
Time frame: Day90
Low molecular weight Heparin (LMWH) 2500 U anti-XA/day or Warfarine 1 mg/day during the first line of chemotherapy
Time frame: Day90
- Detection of asymptomatic thrombosis related to implantable device estimated by a systematic echo-doppler. -
Time frame: Day90
- Frequency of other symptomatic venous thromboembolic events between 3 groups.
Time frame: J0, J1, J21, J42, J63 and J90
Comparison of thrombosis prophylaxis by LMWH with warfarin at low dose
Time frame: Day90
-Costs in the 3 strategies
Time frame: J90
- Tumoral response to chemotherapy in the 3 groups.
Time frame: Day90
- Overall survival in each group.
Time frame: Day90
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