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NOT YET RECRUITING
NCT06850337

Megakaryocyte Heterogeneity in Sickle Cell Disease

Sponsor: Centre Hospitalier Universitaire de la Guadeloupe

View on ClinicalTrials.gov

Summary

Sickle cell disease (SCD) is characterized by chronic hemolytic anemia, painful crisis called vaso-occlusive crisis (VOC) and chronic inflammation. Activated platelets of SCD patients participated to both chronic inflammation and painful VOC. Platelets are anucleated cells from the fragmentation of megakaryocytes in bone marrow. The main aim of this study is to characterize the distribution of the different megakaryocyte subpopulations of sickle cell disease patients SS and SC and in particular the "immune" megakaryocytes CD148+CD48+ and to compare it with the platelet phenotype.

Official title: Characterization of Megakaryocytic Subpopulations and the "Immune" Phenotype of Platelets of the Sickle Cell Disease Patient

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

100

Start Date

2025-07

Completion Date

2027-03

Last Updated

2025-05-25

Healthy Volunteers

Yes

Locations (1)

Chu de La Guadeloupe

Pointe-à-Pitre, Guadeloupe