Phenotypic and Transcriptomic Description of Megakaryocytes in Sickle Cell Patient
NCT06887907 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 40
Last updated 2025-03-20
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.
Conditions
- Sickle Cell Disease (SCD)
Sponsors & Collaborators
-
University Hospital, Toulouse
lead OTHER
Principal Investigators
-
Pierre COUGOUL, MD · University Hospital, Toulouse
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2025-03-13
- Primary Completion
- 2027-04-01
- Completion
- 2028-04-01
Countries
- France
Study Locations
More Related Trials
-
Hemostasis in Sickle Cell Disease--Infancy to Adulthood
NCT00005703 ·Status: COMPLETED
-
Evaluation of the Impact of Red Blood Cell Exchange on Thrombo-inflammation in Sickle Cell Disease
NCT06769139 ·Status: NOT_YET_RECRUITING
-
Study of Erythrocyte Parameters and Hypercoagulability in Sickle Cell Disease (SCD-TGA)
NCT05376046 ·Status: RECRUITING
-
Long-term Endurance Training in Sickle Cell Disease Patients: Impact on Clinical Profile, Physical Fitness, and Quality of Life.
NCT06823219 ·Status: RECRUITING ·Phase: NA
-
Functional and Mechanistic Characterization of Limb Ulcers in Patients With Sickle Cell Disease
NCT04983654 ·Status: COMPLETED ·Phase: NA
-
Study of a Deformability Parameter of Red Blood Cell
NCT05850156 ·Status: NOT_YET_RECRUITING
-
The Influence of micro-and Macro Vascular Dysfunction on Clinical Severity in Adults With Sickle Cell Anemia (SS) and Sickle Cell Hemoglobin C Disease (SC)
NCT07277023 ·Status: COMPLETED ·Phase: NA
-
The Genetics and Functional Basis of Inherited Platelet, White Blood Cell, Red Blood Cell, and Blood Clotting Disorders.
NCT00230165 ·Status: RECRUITING
-
Relationship Between Biological Phenotype, Clinical Severity of Sickle Cell Disease, and Blood Coagulation
NCT06619093 ·Status: NOT_YET_RECRUITING
-
MACS Study - Microparticles and Coagulation in Sickle Cell Disease
NCT01242878 ·Status: UNKNOWN
-
Study of Blood Platelets in Sickle Cell Disease
NCT00226083 ·Status: WITHDRAWN
-
Evaluation of the Hemostatic Potential in Sickle Cell Disease Patients
NCT02565082 ·Status: COMPLETED ·Phase: NA
-
Inflammatory Response to Hydroxyurea Therapy in Sickle Cell Disease
NCT00784082 ·Status: COMPLETED
-
A Pilot Study of Fecal Microbiome and Neutrophil Cellular Adhesion Molecules in Patients With Sickle Cell Disease (SCD)
NCT03007849 ·Status: UNKNOWN
-
Microvascular Blood Flow in Sickle Cell Anemia
NCT01566890 ·Status: COMPLETED ·Phase: NA
-
Pathophysiology of Acute Pain in Patients With Sickle Cell Disease
NCT03049475 ·Status: COMPLETED
-
Evaluation of Impact of Disease on Quality of Life, Education and Socio-professional Integration of Adults and Parents of Children Living with Sickle- Cell Disease in France
NCT04413539 ·Status: COMPLETED
-
SCRIPT: Sickle Cell Risk in Pregnancy Tool
NCT06529042 ·Status: ENROLLING_BY_INVITATION
-
Prognostic Factors of Acute Splenic Sequestration
NCT01207037 ·Status: COMPLETED ·Phase: NA
-
Microvessels and Heart Problems in Sickle Cell Disease
NCT01602809 ·Status: COMPLETED
-
Living With Sickle Cell Disease in the COVID-19 Pandemic
NCT04417673 ·Status: COMPLETED
-
Dense Red Blood Cells in Sickle Cell Children
NCT02887118 ·Status: TERMINATED
-
Children and Adult Hemophagocytic Syndrome (HLHa)
NCT02113917 ·Status: COMPLETED
-
Role of Placenta Growth Factor in Sickle Acute Chest Syndrome
NCT00448370 ·Status: COMPLETED
-
Neutrophil Extracellular Traps and Sickle Cell Disease
NCT02004808 ·Status: UNKNOWN