Universal Rare Gene Study: A Registry and Natural History Study of Retinal Dystrophies Associated With Rare Disease-Causing Genetic Variants

Recruiting

Universal Rare Gene Study: A Registry and Natural History Study of Retinal Dystrophies Associated With Rare Disease-Causing Genetic Variants

Sponsor:

Jaeb Center for Health Research

Code:

NCT05589714

Conditions

Inherited Retinal Degeneration

Retinitis Pigmentosa

Eligibility Criteria

Sex: All

Age: 4+

Healthy Volunteers: Not accepted

Study Details

Eligibility Criteria

Study Design

Interventions and Outcome Measures

Central Contacts and Locations

More Information

Trial information was received from ClinicalTrials.gov and was last updated on 2025-06-16. This information was provided to ClinicalTrials.gov by Jaeb Center for Health Research on 2025-02-10.