Evaluation of non-invasive widefield OCT angiopgraphy in eyes with radiation retinopathy and hypertensive retinopathy

• Conditions: H35.0; Background retinopathy and retinal vascular changes

• Registration Number: DRKS00023390
• Lead Sponsor: niversitätsaugenklinik Kiel

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2020-11-10
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Pending
• Sex: All
• Target Recruitment: 40

Inclusion Criteria

Patients with radiation retinopathy and hypertensive retinopathy where fluorescein angiogrpahy is planned

Exclusion Criteria

- reduced general condition of health, inability to sit through examination
- severe chronic diseases and/or psychic conditions that will severely reduce cooperative participation
- severe optic opacities reducing retinal examinability
- prisoners, institutionalized patients
- confirmed or suspected fluorescein allergy

Study & Design

• Study Type: observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Diagnostic accuracy OCTA vs FAG

Secondary Outcome Measures

Name	Time	Method
Comparison of field of view, unwanted side-effects