Not applicableEnded earlyNCT01802190What this trial is testingPrevalence of POU4F3 and SLC17A8 MutationsWho this might be right forFamilial Deafness University Hospital, Montpellier 50
Not applicableLooking for participantsNCT05917496What this trial is testingAnalysis of Parental Support in Families Using the LENA After Early Cochlear ImplantationWho this might be right forProfound Congenital DeafnessCochlear Implantation Assistance Publique - Hôpitaux de Paris 30
Not applicableStudy completedNCT02294513What this trial is testingHearing Instruments in Alzheimer's DiseaseWho this might be right forAlzheimer DiseaseHearing Loss Phonak AG, Switzerland 25
Not applicableLooking for participantsNCT01793168What this trial is testingRare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at SanfordWho this might be right forRare DisordersUndiagnosed DisordersDisorders of Unknown Prevalence+340 more Sanford Health 20,000
Not applicableStudy completedNCT00481130What this trial is testingAlport Syndrome Treatments and Outcomes RegistryWho this might be right forAlport Syndrome University of Minnesota 655
Not applicableNot Yet RecruitingNCT07782177What this trial is testingOptimizing Elderly Hearing Loss Care in Hong Kong A Cost-Effectiveness and Satisfactory Analysis of a Pilot Collaborative Model Between Otorhinolaryngologists and Family Medicine SpecialistsWho this might be right forHearing Loss, Age-RelatedPresbycusis Tseung Kwan O Hospital, Hong Kong 500
Not applicableStudy completedNCT03483428What this trial is testingAdaptation and Pilot Testing of a Behavioral Parent Training Program for Parents of Deaf and Hard of Hearing ChildrenWho this might be right forHearing LossBehavior DisordersParenting University of Kentucky 6
Testing effectiveness (Phase 2)Ended earlyNCT05085964What this trial is testingAn Open-Label Extension Study to Evaluate Safety & Tolerability of QR-421a in Subjects With Retinitis PigmentosaWho this might be right forRetinitis PigmentosaUsher Syndrome Type 2 Laboratoires Thea 21
Not applicableTemporarily pausedNCT05118867What this trial is testingImprove the Patients' Recovery With Family- Caregivers to End DeliriumWho this might be right forDelirium Mayo Clinic 120
Not applicableLooking for participantsNCT06944171What this trial is testingEffects of Associated Impairments on Activity and Participation in Children With Cerebral PalsyWho this might be right forCerebral Palsy Hacettepe University 107
Not applicableActive Not RecruitingNCT03916146What this trial is testingBehavioral Parent Training for Families With Deaf and Hard of Hearing PreschoolersWho this might be right forDeafnessHearing LossParenting+1 more Christina Studts 295
Not applicableActive Not RecruitingNCT04988451What this trial is testingFamily ASL: Longitudinal Study of Deaf Children and Hearing Parents Who Receive Services to Support the Learning of ASLWho this might be right forDeafnessHearing Loss University of Connecticut 40
Not applicableLooking for participantsNCT06065852What this trial is testingNational Registry of Rare Kidney DiseasesWho this might be right forAdenine Phosphoribosyltransferase DeficiencyAH AmyloidosisAHL Amyloidosis+81 more UK Kidney Association 35,000
Not applicableUnknownNCT03557879What this trial is testingExome Analysis in Hearing Impaired PatientsWho this might be right forHearing Impairment University Hospital, Montpellier 30
Not applicableUnknownNCT05970445What this trial is testingClinical Phenotypic Characteristics of SC26A4Who this might be right forHearing LossPendred Syndrome Chinese PLA General Hospital 300
Not applicableEnrolling By InvitationNCT06938542What this trial is testingPalliative Care Needs of Children With Rare Diseases and Their FamiliesWho this might be right forTrisomy 13 SyndromeArthrogryposis Congenita Multiplex With Intestinal AtresiaAsparagine Synthetase Deficiency+16 more Children's National Research Institute 480
Not applicableActive Not RecruitingNCT03655223What this trial is testingEarly Check: Expanded Screening in NewbornsWho this might be right forSpinal Muscular AtrophyFragile X SyndromeFragile X - Premutation+182 more RTI International 30,000
Not applicableLooking for participantsNCT01694940What this trial is testingNorth American Mitochondrial Disease Consortium Patient Registry and Biorepository (NAMDC)Who this might be right forMitochondrial DisordersMitochondrial Genetic DisordersMitochondrial Diseases+2 more Columbia University 1,000