Not applicableActive Not RecruitingNCT04285398What this trial is testingProspective Natural History Study of Retinitis PigmentosaWho this might be right forRetinitis Pigmentosa SparingVision 82
Not applicableEnded earlyNCT03968991What this trial is testingVISIODOL: Validation of the VISIODOL® ScaleWho this might be right forVisual DeficiencyCongenital BlindnessAcquired Blindness University Hospital, Clermont-Ferrand 37
Not applicableLooking for participantsNCT02435940What this trial is testingInherited Retinal Degenerative Disease RegistryWho this might be right forEye Diseases HereditaryRetinal DiseaseAchromatopsia+25 more Foundation Fighting Blindness 20,000
Not applicableStudy completedNCT02909985What this trial is testingVisual Activity Evoked by Infrared in Humans After Dark AdaptationWho this might be right forAge Related Macular DegenerationRetinitis PigmentosaCongenital Stationary Night Blindness+1 more University of New Mexico 21
Early research (Phase 1)Study completedNCT00821340What this trial is testingClinical Trial of Gene Therapy for Leber Congenital Amaurosis Caused by RPE65 MutationsWho this might be right forLeber Congenital Amaurosis Hadassah Medical Organization 3
Post-approval studies (Phase 4)Ended earlyNCT00634972What this trial is testingEfficient Study of ACULAR in Inhibiting Proliferative Retinopathy in PrematurityWho this might be right forRetinopathy of PrematurityRetinal DetachmentBlindness University of South Alabama 83
Not applicableLooking for participantsNCT03988764What this trial is testingMonogenic Diabetes Misdiagnosed as Type 1Who this might be right forDiabetes Mellitus, Type 1Monogenic DiabetesNeonatal Diabetes+4 more McGill University Health Centre/Research Institute of the McGill University Health Centre 5,000
Large-scale testing (Phase 3)UnknownNCT04855045What this trial is testingAn Open-label, Dose Escalation and Double-masked, Randomized, Controlled Trial Evaluating Safety and Tolerability of Sepofarsen in Children (<8 Years of Age) With LCA10 Caused by Mutations in the CEP290 Gene.Who this might be right forLeber Congenital Amaurosis 10BlindnessLeber Congenital Amaurosis+8 more ProQR Therapeutics 15
Testing effectiveness (Phase 2)UnknownNCT04940572What this trial is testingEfficacy Study of Daily Administration of VPA in Patients Affected by Wolfram SyndromeWho this might be right forWolfram Syndrome Centre d'Etude des Cellules Souches 23
Not applicableUnknownNCT03990727What this trial is testingPhenotype Correlates Genotype of Inherited Retina Dystrophies, Retinitis Pigmentosa, Con>Rod Dystrophies.Who this might be right forRetinitis PigmentosaCone DystrophyUsher Syndromes+1 more MejoraVisionMD 17,000
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 applicableStudy completedNCT02575430What this trial is testingNatural History Study in Inherited Retinal Disease Subjects Caused by Mutations in RPE65 or LRATWho this might be right forLeber Congenital Amaurosis (LCA)Retinitis Pigmentosa (RP) QLT Inc. 59
Not applicableStudy completedNCT02946879What this trial is testingLong-Term Follow-Up Gene Therapy Study for Leber Congenital Amaurosis OPTIRPE65 (Retinal Dystrophy Associated With Defects in RPE65)Who this might be right forLeber Congenital Amaurosis (LCA)Eye DiseasesEye Diseases, Hereditary+1 more MeiraGTx UK II Ltd 15
Not applicableStudy completedNCT03319524What this trial is testingClinical and Genetic Testing of Patients With Usher SyndromeWho this might be right forUsher SyndromeCongenital DeafnessRetinitis Pigmentosa Sensor Technology for Deafblind 28
Not applicableStudy completedNCT02970266What this trial is testingGenetic Decryption of Leber Congenital Amaurosis (LCA) in a Large Cohort of Independent Families.Who this might be right forLeber Congenital Amaurosis Assistance Publique - Hôpitaux de Paris 659
Not applicableStudy completedNCT00106743What this trial is testingNatural History and Genetic Studies of Usher SyndromeWho this might be right forRetinitis Pigmentosa SyndromicCongenital DeafnessUsher Syndrome+2 more National Eye Institute (NEI) 249
Early research (Phase 1)Study completedNCT00516477What this trial is testingSafety Study in Subjects With Leber Congenital AmaurosisWho this might be right forLeber Congenital Amaurosis Spark Therapeutics, Inc. 12
Not applicableUnknownNCT03975543What this trial is testingRetrospective Natural History Study of Retinitis PigmentosaWho this might be right forRetinitis Pigmentosa (RP) SparingVision 113
Very early researchStudy completedNCT01109576What this trial is testingWorkshops for Veterans With Vision and Hearing LossWho this might be right forDeafnessBlindness US Department of Veterans Affairs 13
Large-scale testing (Phase 3)Study completedNCT01203436What this trial is testingSupplemental Therapeutic Oxygen for Prethreshold Retinopathy of PrematurityWho this might be right forInfant, NewbornInfant, Low Birth WeightInfant, Small for Gestational Age+3 more NICHD Neonatal Research Network 649