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Clinical Trial Summary

Idiopathic thrombocytopenic purpura (ITP) is the most frequent auto-immune cytopenia. There is no specific biological marker and the diagnosis often results from the exclusion of other differential diagnoses, notably inherited thrombocytopenia. Recent studies have reported an original platelet destruction mechanism in ITP, by antibody-mediated desialylation of membrane proteins. The detection of platelet sialylation can be readily achieved using flow cytometry. This could provide a new biomarker of ITP, useful to ascertain a diagnosis of ITP and guide towards proper patient management.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03421392
Study type Observational
Source Nantes University Hospital
Contact
Status Completed
Phase
Start date January 1, 2018
Completion date November 1, 2020

See also
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