[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Tobias Moser\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":40},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"id":9,"slug":4,"hasResults":10,"nctId":11,"briefTitle":12,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":10,"sex":15,"minAge":4,"maxAge":4,"enrollmentInfo":16,"targetDuration":19,"studyType":20,"phases":4,"briefSummary":21,"conditions":22,"keywords":25,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":29,"lastUpdatePostDateStruct":30,"startDateStruct":33,"completionDateStruct":35,"leadSponsor":37,"locationsCount":5},"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":17,"type":18},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.",[23,24],"Otoferlin-related Auditory Synaptopathy","Hearing Impairment",[26,27],"Otoferlin patient registry","Natural history study","RECRUITING","2025-05-21",{"date":31,"type":32},"2025-05-28","ACTUAL",{"date":34,"type":32},"2023-02-21",{"date":36,"type":18},"2048-02-21",{"name":38,"class":39},"Tobias Moser","OTHER",""]