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Recruiting Observational

National Exhaustive Cohort of Hereditary Stomatocytoses and Other Channelopathies Affecting the Red Blood Cell

NCT04778657 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2021-05-06
Last updated
2021-11-03

Condition(s) studied

Stomatocytosis

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

Sex
ALL
Min age
—
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Any patient with a diagnosis of stomatocytosis without age limit * Patient affiliated or beneficiary of french Social Security * No objection from the patient or legal representative Exclusion Criteria: * Diagnosis of stomatocytosis excluded by ektacytometry and / or genetics * Patient under guardianship, with curators or legal protection

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)

FacilityCityRegionStatus
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
Official registry record

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