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Evaluation of the Repeatability and Reproducibility of AngioVue

O

Optovue

Status

Completed

Conditions

Normal, Glaucoma & Retinal Pathology

Treatments

Device: Optical Coherence Tomography Angiography

Study type

Observational

Funder types

Industry

Identifiers

NCT02911883
200-51133

Details and patient eligibility

About

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.

Enrollment

70 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Normal

    • Age > 18.
    • No retinal pathology or glaucoma.
  2. Glaucoma patient

    • Age > 18.
    • Have glaucoma.
  3. Retina patient

    • Age > 18.
    • Have retina pathology.

Exclusion criteria

  1. Normal

    • Unable to complete required exams.
    • Poor quality image data.
  2. Glaucoma patient

    • Unable to complete required exams.
    • Poor quality image data.
    • Retinal pathology.
  3. Retina patient

    • Unable to complete required exams.
    • Poor quality image data.
    • Glaucoma.

Trial design

70 participants in 3 patient groups

Normal
Description:
Not having glaucoma or retinal pathology
Treatment:
Device: Optical Coherence Tomography Angiography
Glaucoma
Description:
Having glaucoma.
Treatment:
Device: Optical Coherence Tomography Angiography
Retina
Description:
Having retinal pathology
Treatment:
Device: Optical Coherence Tomography Angiography

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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