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Recruiting Observational

Phenotypic and Transcriptomic Description of Megakaryocytes in Sickle Cell Patient

NCT06887907 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2025-03-13
Last updated
2025-03-20

Condition(s) studied

Sickle Cell Disease (SCD)

Study summary

Sickle cell disease is the most common inherited blood disorder in the world. Chronic hemolysis induces platelet activation and chronic inflammation. Platelets and megakaryocyte, as medullar platelets precursors, are known to play a role in innate immunity. Little is known about the role of megakaryocytes at basal state and during acute complication in sickle cell disease patients. The aim of this study is to evaluate the role of megakaryocytes in sickle cell disease.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Sickle cell disease SS or S-béta° thalassemia * Patient at steady state since at least 1 year or at steady state (without crisis), or during vaso-occlusive crisis or during acute chest syndrome * Age \> 18 years old Exclusion Criteria: * Patient objects to take part in the study Hematologic disorder (leukemia, myeloma, myelodysplasic syndrome, myeloproliferative syndrome) * Immune thrombocytopenia, Immunosuppressive or anti-inflammatory (biotherapies, corticosteroids, non steroidal anti-inflammatories drugs) Page 12 sur 23 * Anti-platelets agents * Red blood cell exchange or transfusion \< 3 months

Primary outcome measure(s)

  • Description of circulant megakaryocytes — 12 months
    Phenotypic and transcriptomic description of circulant megakaryocytes in sickle cell patient

Trial sites (1)

FacilityCityRegionStatus
CHU de Toulouse Toulouse France Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06887907 on ClinicalTrials.gov ↗ ← All trials in France