cone-rod dystrophy 'inherited retinal diseases' Leber congenital amaurosis retinitis pigmentosa Stargardt disease
Conditions
Interventions
None listed
Sponsors
Universitair Medisch Centrum Sint Radboud
Eligibility
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: -Patients recruited from the RP5000 study (see Onderzoeksprotocol, page 7 + 8) with one of the following non-syndromic retinal dystrophies: Retinitis pigmentosa, Leber congenital amaurosis, Stargardt disease or cone-rod dystrophy. -Healthy independent volunteers with normal retinal functionality. -All study participants are of mature age and of sound mind and judgement. -Both eyes are able to fixate adequately for the imaging procedure. -Absence of cataract in both eyes.
Exclusion criteria
Exclusion criteria: Healthy volunteers and patients, who do not meet the inclusion criteria.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Identification and classification of optical features that indicate the functionality of the retina in healthy individuals and in patients with retinal dystrophies. | — |
Secondary
| Measure | Time frame |
|---|---|
| Not applicable. | — |
Countries
Netherlands
Outcome results
None listed