Trials / NCT05258032
Structural and Functional Characterization of Rare Ocular Diseases
Status unknown Observational Natural history / observational
- Sponsor
- Barcelona Macula Foundation
- Treatment
- Not listed
- Gene
- Not stated
- Conditions
- Retinitis Pigmentosa, Stargardt Disease 1, Best Disease, Pattern Dystrophy of Macula, Choroideremia
- Ages
- 18 Years to no upper limit
- Enrollment
- 50 participants
- Started
- 2021-11-24
- Main results expected
- 2024-11-24
- Results posted
- Not yet
- Record last updated
- 2022-03-15
What the study is testing
Rare ocular diseases (ROD) are a heterogeneous group of ocular diseases that affect very few people and, generally, for which no tretament is available. An important subgroup of these diseases are inherited retinal degenerations. In this study we focus on understanding the natural history of different ROD that affect the posterior segment.
Where it runs
Spain (1)
- Institut de la màcula, Barcelona (recruiting now)