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Thrombophilia In Beta Thalassemia
Sponsor: Assiut University
Summary
β-thalassemia disease is one of the most common congenital hemolytic anemia commonly found in the malarial belt areas including the Mediterranean, the Middle East, Africa, Southeast Asian countries, and China.
Official title: Thrombophilia Versus Platelet Dysfunction In Beta Thalassemia
Key Details
Gender
All
Age Range
4 Years - 20 Years
Study Type
OBSERVATIONAL
Enrollment
100
Start Date
2024-05-07
Completion Date
2024-05-31
Last Updated
2024-05-07
Healthy Volunteers
Not specified
Conditions
Interventions
PT
measuring PT drawn on citrated blood sample
Protein C
measuring protein C drawn on citrated blood sample
Platelet aggregation by ADP and arachidonic acid
measuring platelet aggregation drawn on citrated blood sample