[{"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":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":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":32,"startDateStruct":35,"completionDateStruct":37,"leadSponsor":39,"locationsCount":5},"100568416","cabp2-patient-registry-and-natural-history-study-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":18,"type":19},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.",[24,25],"CABP2-related Auditory Synaptopathy","Hearing Impairment",[27,28,29],"CABP2 patient registry","Patient registry","DFNB93","RECRUITING","2026-01-23",{"date":33,"type":34},"2026-01-27","ACTUAL",{"date":36,"type":34},"2024-08-16",{"date":38,"type":19},"2049-08-16",{"name":40,"class":41},"University Medical Center Goettingen","OTHER"]