National Exhaustive Cohort of Hereditary Stomatocytoses and Other Channelopathies Affecting the Red Blood Cell
Condition(s) studied
Study 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
Eligibility
Primary outcome measure(s)
- Obtain a description of the clinical and laboratory data of patients at the time of diagnosis of stomatocytosis — Baseline
Descriptive analysis of clinical and biological data for the diagnosis of stomatocytosis
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| AP-HP, Bicêtre Hospital, Pediatrics - Hematology - Reference center for Sickle cell anemia, Thalassemia and other constitutional diseases of the red blood cell | Le Kremlin-Bicêtre | France | Recruiting |
More Assistance Publique - Hôpitaux de Paris trials in France
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT04778657 on ClinicalTrials.gov ↗ ← All trials in France