NCT Number: NCT02911883
Evaluation of the Repeatability and Reproducibility of AngioVue
The purpose of this study is to assess the repeatability and reproducibility of measurements of the vascular structures and the anatomical structures of the posterior pole of the eye based on AngioVue volume scans in normal subjects, glaucoma patients, and retina patients.
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Notify MeKey information
Age range
18 year and older
Sex eligibility
All sexes
Study type
Observational
Who can participate
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Normal
- Age > 18.
- No retinal pathology or glaucoma.
- Glaucoma patient
- Age > 18.
- Have glaucoma.
- Retina patient
- Age > 18.
- Have retina pathology.
Exclusion criteria
- Normal
- Unable to complete required exams.
- Poor quality image data.
- Glaucoma patient
- Unable to complete required exams.
- Poor quality image data.
- Retinal pathology.
- Retina patient
- Unable to complete required exams.
- Poor quality image data.
- Glaucoma.
Treatment and study plan
Primary outcomes
-
Retina vasculature
Time frame: Day 1
Sponsors and collaborators
Lead sponsor
Optovue
Industry
Registry information
Important dates
- Study start
- 2016
- Primary completion
- 2017
- Study completion
- 2017
- First posted
- Sep 22, 2016
- Registry last updated
- Jun 20, 2017
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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