This study is designed to provide efficacy and safety data for certoparin in the prophylaxis of venous thromboembolism in immobilized, acutely ill medical patients.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
TRIPLE
Enrollment
3,254
3000 U anti XA of certoparin in 0.3 ml solution, once daily
solution, 5000 IU of unfractionated heparin in 0.3 ml, 3 times daily
Novartis investigative sites
Nuremberg, Germany
Incidence of venous thromboembolism during treatment (proximal deep vein thrombosis, pulmonary embolism, death related to venous thromboembolism)
Time frame: 20 days
proximal and distal deep vein thrombosis (DVT) (combined and separate) assessed by ultrasound screening,
Time frame: 20 days
symptomatic DVT,
Time frame: 20 days
symptomatic non-fatal pulmonary embolism (PE),
Time frame: 20 days
combination of proximal DVT, non fatal PE and death from all causes including PE
Time frame: 20 days
VTE related death,
Time frame: 20 days
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