University of Kentucky, Advanced Eye Care
Welcome,         Profile    Billing    Logout  
 0 Trials 
6 Trials

   

 
Trial + Data / EventsStatusPhNRegionInterventionsSponsorConditionsPrimary complStudy compl
Maldonado, Ramiro S
Guardian, NCT05956626: Study to Assess the Safety and Efficacy of OCU410ST for Stargardt Disease

Recruiting
1/2
42
US
OCU410ST
Ocugen
Stargardt Disease
10/25
10/25
NCT06139523: Optimize Pediatric OCT Imaging

Recruiting
N/A
30
US
Investigational contact OCT system, Theia 1 widefield imaging system, Investigational noncontact OCT system:, Ultracompact swept source OCT system
Duke University
Retinal Disease, Glaucoma, Optic Nerve Diseases
07/25
12/25
SS-HH-OCT, NCT06177977: as a Novel Diagnostic Modality for Early-Onset Retinal Dystrophies (EORDs)

Recruiting
N/A
80
US
SS-HH-OCT, Swept-source Handheld Ultracompact Optical Coherence Tomography (HH UC OCT)
Duke University
Retinal Dystrophies
12/26
12/26
POLARIS, NCT06435000: An Observational Study in Subjects to Follow the Progression of Stargardt Disease Type 1 (STGD1) Caused by Bi-Allelic Autosomal Recessive Mutations in the ABCA4 Gene

Recruiting
N/A
75
Europe, US
Splice Bio
Stargardt, Stargardt's Disease, Stargardt Disease, STGD1
12/26
02/27
RUSH1F, NCT04765345: Rate of Progression of PCDH15-Related Retinal Degeneration in Usher Syndrome 1F

Active, not recruiting
N/A
40
Europe, Canada, US, RoW
Jaeb Center for Health Research, Usher 1F Collaborative, Marjorie C. Adams Foundation, Foundation Fighting Blindness
Retinal Degeneration, Retinitis Pigmentosa, Eye Diseases, Hereditary
06/27
06/27
Uni-Rare, NCT05589714: Universal Rare Gene Study: A Registry and Natural History Study of Retinal Dystrophies Associated With Rare Disease-Causing Genetic Variants

Recruiting
N/A
1500
Europe, Canada, US, RoW
Jaeb Center for Health Research, Foundation Fighting Blindness
Inherited Retinal Degeneration, Retinitis Pigmentosa
12/28
12/28

Download Options