Functional Retinal Imaging of Inherited Retinal Diseases

Withdrawn

• Conditions: cone-rod dystrophy; 'inherited retinal diseases'; Leber congenital amaurosis; retinitis pigmentosa; Stargardt disease; 10015920; 10010463

• Registration Number: NL-OMON37165
• Lead Sponsor: niversitair Medisch Centrum Sint Radboud

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 29 April 2024

Recruitment & Eligibility

• Status: Withdrawn
• Sex: Not specified
• Target Recruitment: 40

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

Healthy volunteers and patients, who do not meet the inclusion criteria.

Study & Design

• Study Type: Observational non invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Identification and classification of optical features that indicate the<br /><br>functionality of the retina in healthy individuals and in patients with retinal<br /><br>dystrophies.</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Not applicable.</p><br>