[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"otoferlin-related-auditory-synaptopathy\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:otoferlin-related-auditory-synaptopathy":24},{"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":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":4,"maxAge":4,"enrollmentInfo":17,"targetDuration":20,"studyType":21,"phases":4,"briefSummary":22,"conditions":23,"keywords":26,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":30,"lastUpdatePostDateStruct":31,"startDateStruct":34,"completionDateStruct":36,"leadSponsor":38,"locationsCount":5},"100511946","otoferlin-patient-registry-and-natural-history-study-100511946",false,"NCT05946057","Otoferlin Patient Registry and Natural History Study","Patient Registry for Individuals With Otoferlin-Associated Hearing Loss","Inclusion Criteria:\n\n* A molecular genetic diagnosis involving biallelic variants in otoferlin (OTOF) and audiometry\n\nExclusion Criteria:\n\n* Patients with evidence of non-OTOF molecular genetic diagnoses","ALL",{"count":18,"type":19},100,"ESTIMATED","25 Years","OBSERVATIONAL","This registry is designed to collect comprehensive information about the molecular genetic diagnoses of individuals with otoferlin-associated hearing impairment and clinical information to support a natural history study.",[24,25],"Otoferlin-related Auditory Synaptopathy","Hearing Impairment",[27,28],"Otoferlin patient registry","Natural history study","RECRUITING","2025-05-21",{"date":32,"type":33},"2025-05-28","ACTUAL",{"date":35,"type":33},"2023-02-21",{"date":37,"type":19},"2048-02-21",{"name":39,"class":40},"Tobias Moser","OTHER"]