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Clinical Trial Summary

Hereditary stomatocytosis is a heterogeneous group of rare constitutional diseases of dominant transmission in the vast majority of cases. The data concerning their clinical and biological presentation, and their evolution are few, and come from about thirty clinical cases. The constitution of an exhaustive French cohort of hereditary stomatocytosis will improve the establishment of the diagnosis and the management of patients


Clinical Trial Description

The patient is prospectively included. The referring hematologist will inform the patient about participation in the cohort, give him the information note and obtain his non-objection agreement to the use of his data for research purposes. The data will be collected from the medical file of each patient as part of his usual annual follow-up. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04778657
Study type Observational [Patient Registry]
Source Assistance Publique - Hôpitaux de Paris
Contact Corinne GUITTON, MD,PhD
Phone 01 45 21 32 47
Email corinne.guitton@aphp.fr
Status Recruiting
Phase
Start date May 6, 2021
Completion date March 1, 2041