Evolution of Thromboelastography During Tranexamic Acid Treatment
Launched by CENTRE HOSPITALIER UNIVERSITAIRE DE SAINT ETIENNE · Jan 10, 2019
Trial Information
Current as of June 16, 2025
Completed
Keywords
ClinConnect Summary
Patients with hematological malignancies often develop low platelet counts either as a consequence of the disease or the treatment by chemotherapy or stem cell transplantation. Platelet transfusions are commonly given to raise any low platelet count and reduce the risk of clinical bleeding (prophylaxis) or stop active bleeding (therapy). The last studies have showed that many patients continue to experience bleeding, despite the use of platelet transfusions. Tranexamic acid is an antifibrinolytic agent. It reduces the breakdown of clots formed. This treatment is widely used in medicine (e.g...
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Patient affiliated to a social security regimen or beneficiary of the same
- • Signed written informed consent form
- • Confirmed diagnosis of a hematological malignancy and undergoing intensive chemotherapy
- • Expected to experience hypoproliferative thrombocytopenia resulting in a platelet count of ≤10 G/L for ≥ 5 days
- Exclusion Criteria:
- • Pregnant women
- • Patient under guardianship or deprived of his liberty or any condition that may affect the patient's ability to understand and sign the informed consent
- • Refractoriness to platelet transfusion or requirement for a specific type of platelet transfusion (ABO-compatible, plasma-free)
- • Ongoing anticoagulant therapy or antiplatelet therapy at the time of enrolment
- • Treatment with any pro-coagulant agent within 48 hours of enrolment, or enrolment in other trials involving platelet transfusions, platelet growth factors, or presentation of a known hypercoagulable state
- • Diagnosis of arterial or venous thromboembolic disease within the previous year
- • Patient experiencing a bleeding event WHO grade ≥ 2 within 7 days before inclusion
- • contra-indications to tranexamic acid (allergy, history of seizures, creatinine clearance \< 30 mL/min)
- • Refusing participation
About Centre Hospitalier Universitaire De Saint Etienne
The Centre Hospitalier Universitaire (CHU) de Saint-Étienne is a leading academic medical center in France, dedicated to advancing healthcare through innovative clinical research and high-quality patient care. With a robust infrastructure that supports a wide range of medical specialties, CHU de Saint-Étienne fosters collaboration between healthcare professionals, researchers, and academic institutions. The center is committed to conducting rigorous clinical trials that adhere to ethical standards and regulatory requirements, aiming to improve treatment outcomes and enhance the overall health of the community. Through its dedication to scientific excellence and patient-centered care, CHU de Saint-Étienne plays a pivotal role in the advancement of medical knowledge and the development of new therapeutic interventions.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Saint étienne, , France
Patients applied
Trial Officials
Emilie Chalayer, MD
Principal Investigator
CHU de Saint-Etienne
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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