Scientists map the path of a rare blinding disease
NCT ID NCT04765345
Summary
This study aims to understand how quickly vision declines in people with a specific genetic cause of Usher syndrome, a condition that causes both hearing and vision loss. Researchers will follow 44 participants with PCDH15 gene mutations for four years, measuring their vision and eye structure in detail. The goal is to gather essential information to help design and measure the success of future treatment trials.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes NO responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for RETINITIS PIGMENTOSA are added.
By submitting, you agree to our Terms of use
Contacts and locations
Show contact details
Enter your email to view the contact information for this study.
By submitting, you agree to our Terms of use
Locations
-
CHNO des Quinze-Vingts
Paris, France
-
Duke University, Duke Eye Center
Durham, North Carolina, 27710, United States
-
Haddassah Medical Center
Jerusalem, Israel
-
Hospital for Sick Children
Toronto, Ontario, Canada
-
Moorfields Eye Hospital
London, EC1V 2PD, United Kingdom
-
Radboud University
Nijmegen, Netherlands
-
The Johns Hopkins Wilmer Eye Institute
Baltimore, Maryland, 21287, United States
-
University Hospital Basel
Basel, 4031, Switzerland
-
University of California, San Francisco
San Francisco, California, 94143-0344, United States
-
University of Tubingen
Tübingen, Germany
Conditions
Explore the condition pages connected to this study.