[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"dystrophinopathies\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:dystrophinopathies":25},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":23,"conditions":24,"keywords":26,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":32,"startDateStruct":35,"completionDateStruct":37,"leadSponsor":39,"locationsCount":5},"100602621","decoding-central-defects-in-dystrophinopathies-from-diagnostic-to-remediation-100602621",false,"NCT07125898","Decoding Central Defects in Dystrophinopathies From Diagnostic to Remediation","DECODYS","Inclusion Criteria:\n\n* French citizenship, affiliated to the French Social Security,\n* 5 to 12 years old,\n* DMD diagnosis confirmed by a genetic analysis predicting breaking in the reading frame of the DMD gene with knowledge of the limits of the mutation,\n* Follow-up in a French referral or a skills center belonging to Filnemus.\n\nExclusion Criteria:\n\n* Severe intellectual deficiency with IQ \\\u003C 55, and IQ \\\u003C 70 for the deep neurocognitive evaluation (executive and socio-cognitive evaluation),\n* Cataract except if operated (pseudophakic),\n* High intraocular pressure,\n* Cardiac dysfunction with left ventricular ejection fraction \\\u003C 35%,\n* Respiratory dysfunction with force vital capacity \\\u003C 70%,\n* Difficulties in fine motor skills with D3 MFM scale \\\u003C 75%\n* Treatment with methylphenidate: In case of hyperactive patients, the treatment will be transitorily interrupted the week before testing.","ALL","5 Years","12 Years",{"count":20,"type":21},110,"ESTIMATED","OBSERVATIONAL","The study aims to identify a genotype\u002Fphenotype correlation by analyzing more finely the neurodevelopmental disorders in DMD patients.",[25],"Dystrophinopathies",[27,28,29],"Cognitive deficits","Autism-spectrum disorders","Attention deficit hyperactivity Disorder","RECRUITING","2026-09-17",{"date":33,"type":34},"2026-09-22","ACTUAL",{"date":36,"type":34},"2026-09-16",{"date":38,"type":21},"2031-03",{"name":40,"class":41},"Assistance Publique - Hôpitaux de Paris","OTHER"]