Non interventional multi-centric study that will aim in evaluating the efficacy and safety of Fondaparinux in surgical cancer patients, identifying in parallel the most relevant and critical risk factors for Thromboembolism.
Non interventional multi-centric study that will aim in evaluating the efficacy and safety of Fondaparinux in surgical cancer patients, identifying in parallel the most relevant and critical risk factors for Thromboembolism. It is a cohort study, recruiting cancer patients over 18 years of age, who have been diagnosed with cancer for over a period of one year. Exclusion criteria apply as well while all patients can withdraw their participation at any time point.
Study Type
OBSERVATIONAL
Enrollment
400
Ioannis Karaitianos
Athens, Attica, Greece
RECRUITINGNumber of incidents
Observed number of incidents per cancer type
Time frame: One Year
Number of bleeding episodes
The incidence of bleeding episodes by type of cancer
Time frame: One Year
Comparison of results/incidents among groups
Results of treatment in subgroups of patients (for example patients with newly diagnosed cancer or potential cancer or relapse / metastasis of cancer that has been treated before and diagnosed ≥ 1 year)
Time frame: One Year
Evaluation
Evaluation of antithrombotic treatment
Time frame: One Year
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