[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"cabp2-related-auditory-synaptopathy\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:cabp2-related-auditory-synaptopathy":41},{"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":29,"whyStopped":4,"lastUpdateSubmitDate":30,"lastUpdatePostDateStruct":31,"startDateStruct":34,"completionDateStruct":36,"leadSponsor":38,"locationsCount":5},"100568416",false,"NCT06680934","CABP2 Patient Registry and Natural History Study","Patient Registry for Individuals With CABP2-Associated Hearing Loss","Inclusion Criteria:\n\n* A molecular genetic diagnosis involving biallelic variants in CAPB2 and audiometry\n\nExclusion Criteria:\n\n* Patients with evidence of non-CABP2 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 and clinical information of individuals with CABP2-associated hearing impairment to support a natural history study.",[23,24],"CABP2-related Auditory Synaptopathy","Hearing Impairment",[26,27,28],"CABP2 patient registry","Patient registry","DFNB93","RECRUITING","2026-01-23",{"date":32,"type":33},"2026-01-27","ACTUAL",{"date":35,"type":33},"2024-08-16",{"date":37,"type":18},"2049-08-16",{"name":39,"class":40},"University Medical Center Goettingen","OTHER",""]