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Study of Erythrocyte Parameters and Hypercoagulability in Sickle Cell Disease (SCD-TGA) — SCD-TGA  

Sickle Cell Disease Clinical Trial

Official title:
Study of Erythrocyte Parameters and Hypercoagulability in Sickle Cell Disease

Clinical Trial Summary

Sickle cell disease (SCD) is an inherited haemoglobinopathy disorder caused by mutations in HBB gene with amino-acid substitution on β globin chain. The consequence is synthesis of altered haemoglobin S (HbS) which polymerises in red blood cell (RBC) at deoxygenated state. SCD is associated with chronic haemolytic anaemia, vaso-occlusive crisis (VOC) leading to frequent hospitalisation. The aim of the study was to to investigate whether a combination of routine laboratory biomarkers of haemolysis could be used to predict VOC development in confirmed SCD patients.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05376046
Study type Observational [Patient Registry]
Source University Hospital, Rouen
Contact
Status Recruiting
Phase
Start date September 1, 2018
Completion date September 1, 2026
View Details
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