Clinical Trials Directory

Trials / Completed

CompletedNCT02391558

Clinical Evaluation of Noninvasive OCT Angiography Using a Zeiss OCT Prototype to Compare to Fluorescein Angiography

Status
Completed
Phase
Study type
Observational
Enrollment
62 (actual)
Sponsor
Association for Innovation and Biomedical Research on Light and Image · Academic / Other
Sex
All
Age
18 Years – 90 Years
Healthy volunteers
Not accepted

Summary

Clinical evaluation of noninvasive OCT Angiography using a Zeiss OCT Prototype to replace fluorescein angiography.

Detailed description

Fluorescein angiography (FA) is the standard and generally accepted method to identify vascular features in the retina, detecting capillary dropout and neovessel growth. Its value is undeniable and is a routine ophthalmological examination. However, it requires intravenous injection of fluorescein, which can cause nausea, vomiting and, rarely, anaphylaxis and death. New OCT angiography methods can detect, noninvasively red blood cells flow and, therefore, identify well the retinal vasculature. It is crucial and of major interest to evaluate the clinical utility of this new methodology comparing this information with the one obtained from fluorescein angiography.

Conditions

Timeline

Start date
2015-09-01
Primary completion
2016-04-01
Completion
2016-04-01
First posted
2015-03-18
Last updated
2017-03-10

Locations

1 site across 1 country: Portugal

Source: ClinicalTrials.gov record NCT02391558. Inclusion in this directory is not an endorsement.

Clinical Evaluation of Noninvasive OCT Angiography Using a Zeiss OCT Prototype to Compare to Fluorescein Angiography (NCT02391558) · Clinical Trials Directory