RUSH1F
Research type
Research Study
Full title
Rate of Progression of PCDH15-Related Retinal Degeneration in Usher Syndrome 1F (RUSH1F)
IRAS ID
306351
Contact name
Michel Michaelides
Contact email
Sponsor organisation
Jaeb Center for Health Research (JCHR)
Clinicaltrials.gov Identifier
Clinicaltrials.gov Identifier
N/A, N/A
Duration of Study in the UK
4 years, 6 months, 1 days
Research summary
The purpose of this study is to collect information about people with retinal degeneration caused by mutations in the PCDH15 gene of their DNA. We hope to learn about the traits of these people and study what happens to their eyes and vision over time. We hope to use this information to design studies for future treatments of people with PCDH15- related retinal degeneration.
REC name
South Central - Berkshire B Research Ethics Committee
REC reference
21/SC/0404
Date of REC Opinion
14 Jan 2022
REC opinion
Further Information Favourable Opinion