RP Cure Tracker

Trials / NCT03814499

Natural History Study in Subjects With Usher Syndrome

Completed Observational Natural history / observational

Sponsor
Fondazione Telethon
Treatment
Not listed
Gene
Not stated
Conditions
Usher Syndrome, Type 1B
Ages
8 Years to no upper limit
Enrollment
56 participants
Started
2018-06-01
Main results expected
2020-12-30
Results posted
Yes
Record last updated
2024-12-09

What the study is testing

Natural History Study in Subjects With Usher Syndrome ((USH1B) is a multi-centre, longitudinal, observational study designed to evaluate disease progression in subjects with USH1B by several vision-related assessments.

Where it runs

Italy (1)
Netherlands (1)
Spain (1)

Open on ClinicalTrials.gov for contacts and eligibility