Clinical Efficacy of Platelet Transfusion
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorCentre Hospitalier Universitaire de Besancon
About this trial
The aim of this study is to analyze the effect of the storage time of platelet concentrates on the occurrence of bleeding events during prophylactic platelet transfusions in patients with hematological malignancies.
Eligibility criteria
Qualifiers
Patients with haematological malignancies or bone marrow aplasia with severe thrombocytopenia due to bone marrow failure related to the disease or treatments received
Severe thrombocytopenia requiring transfusion
Patient able to self-assess bleeding events
Non-opposition of the subject to participate in the study
Disqualifiers
Acute promyelocytic leukaemia
Curative dosage of anticoagulants
Treatment with antiplatelet agents
Patient with proven thrombocytopenia of immunological origin, or disseminated intravascular coagulation
Trial design
Treatments tested in this trial
- Self-assessment of bleeding events
Treatment groups
343 Participants
are divided into 1 treatment groupSponsors and collaborators
Source ClinicalTrials.gov