[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100422271":3},{"organization":4,"armGroups":7,"interventions":7,"overallOfficials":8,"centralContacts":13,"locations":19,"responsibleParty":37,"collaborators":7,"id":39,"slug":40,"hasResults":41,"nctId":42,"briefTitle":43,"officialTitle":43,"acronym":44,"eligibilityCriteria":45,"healthyVolunteers":41,"sex":46,"minAge":7,"maxAge":7,"enrollmentInfo":47,"targetDuration":50,"studyType":51,"phases":7,"briefSummary":52,"conditions":53,"keywords":55,"overallStatus":22,"whyStopped":7,"lastUpdateSubmitDate":57,"lastUpdatePostDateStruct":58,"startDateStruct":61,"completionDateStruct":63,"leadSponsor":65,"locationsCount":66},{"fullName":5,"class":6},"Assistance Publique - Hôpitaux de Paris","OTHER",null,[9],{"name":10,"affiliation":11,"role":12},"Corinne GUITTON","APHP","PRINCIPAL_INVESTIGATOR",[14],{"name":15,"role":16,"phone":17,"phoneExt":7,"email":18},"Corinne GUITTON, MD,PhD","CONTACT","01 45 21 32 47","corinne.guitton@aphp.fr",[20],{"facility":21,"status":22,"city":23,"state":7,"zip":24,"country":25,"countryCode":26,"cosmosGeoPoint":27,"geoPoint":32,"contacts":33},"AP-HP, Bicêtre Hospital, Pediatrics - Hematology - Reference center for Sickle cell anemia, Thalassemia and other constitutional diseases of the red blood cell","RECRUITING","Le Kremlin-Bicêtre","94275","France","FR",{"type":28,"coordinates":29},"Point",[30,31],2.36073,48.81471,{"lat":31,"lon":30},[34],{"name":35,"role":16,"phone":36,"phoneExt":7,"email":18},"Corinne GUITTON, MD","+33 (0) 1 45 21 32 47",{"type":38,"investigatorFullName":7,"investigatorTitle":7,"investigatorAffiliation":7,"oldNameTitle":7,"oldOrganization":7},"SPONSOR","100422271","national-exhaustive-cohort-of-hereditary-stomatocytoses-and-other-channelopathies-affecting-the-red-blood-cell-100422271",false,"NCT04778657","National Exhaustive Cohort of Hereditary Stomatocytoses and Other Channelopathies Affecting the Red Blood Cell","COHSTO","Inclusion Criteria:\n\n* Any patient with a diagnosis of stomatocytosis without age limit\n* Patient affiliated or beneficiary of french Social Security\n* No objection from the patient or legal representative\n\nExclusion Criteria:\n\n* Diagnosis of stomatocytosis excluded by ektacytometry and \u002F or genetics\n* Patient under guardianship, with curators or legal protection","ALL",{"count":48,"type":49},150,"ESTIMATED","15 Years","OBSERVATIONAL","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",[54],"Stomatocytosis",[56],"rare genetic disease","2021-10-28",{"date":59,"type":60},"2021-11-03","ACTUAL",{"date":62,"type":60},"2021-05-06",{"date":64,"type":49},"2041-03-01",{"name":5,"class":6},1]