Chronic Idiopathic Thrombocytopenic Purpura Clinical Trial
Official title:
Development of an Approach for the Differential Diagnosis of Chronic Idiopathic Thrombocytopenic Purpura and Congenital Thrombocytopenia
The objective of this study is to provide simple and relevant clinical and biological elements to distinguish a possible Congenital Thrombocytopenia from a Chronic Idiopathic Thrombocytopenic Purpura .
Congenital Thrombocytopenia is a group of rare diseases, often unrecognized and misdiagnosed
as Chronic Idiopathic Thrombocytopenic Purpura. These Chronic Idiopathic Thrombocytopenic
Purpura, which are exclusion diagnoses, are most often treated with corticosteroids or
intravenous immunoglobulins and sometimes, when thrombocytopenia is refractory, splenectomy
is performed. Currently, it is often before a case of thrombocytopenia refractory to the
treatment of the dysimmunity syndrome that the notion of Congenital Thrombocytopenia is
evoked. The percentage of false diagnoses (misdiagnosed Chronic Idiopathic Thrombocytopenic
Purpura diagnoses) seems to represent to date 10 to 20% of cases.
The objective of this study is to provide simple and relevant clinical and biological
elements to distinguish a possible Congenital Thrombocytopenia from a Chronic Idiopathic
Thrombocytopenic Purpura.
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Status | Clinical Trial | Phase | |
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Completed |
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