Actively Recruiting
National Exhaustive Cohort of Hereditary Stomatocytoses and Other Channelopathies Affecting the Red Blood Cell
Led by Assistance Publique - Hôpitaux de Paris · Updated on 2021-11-03
150
Participants Needed
1
Research Sites
1034 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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
CONDITIONS
Official Title
National Exhaustive Cohort of Hereditary Stomatocytoses and Other Channelopathies Affecting the Red Blood Cell
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 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
You will not qualify if you...
- Diagnosis of stomatocytosis excluded by ektacytometry and / or genetics
- Patient under guardianship, with curators or legal protection
AI-Screening
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Trial Site Locations
Total: 1 location
1
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, 94275
Actively Recruiting
Research Team
C
Corinne GUITTON, MD,PhD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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