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Evaluation of the Repeatability and Reproducibility of OCTA Image Quality With the Heidelberg Engineering SPECTRALIS With OCT Angiography Module

Evaluation of the Repeatability and Reproducibility of OCTA Image Quality With the Heidelberg Engineering SPECTRALIS With OCT Angiography Module

Status
Terminated
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03530449
Enrollment
39
Registered
2018-05-21
Start date
2018-04-30
Completion date
2018-09-15
Last updated
2019-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Retinal Vascular, Normal Eyes

Brief summary

Repeatability and Reproducibility of OCTA Image Quality with the Heidelberg Engineering SPECTRALIS

Detailed description

The objectives of this study are to: 1. Assess the repeatability and reproducibility of the SPECTRALIS with OCTA Module image quality 2. Assess the repeatability and reproducibility of visibility of key anatomical vascular structures in the SPECTRALIS with OCTA Module

Interventions

OCT Angiography offers clinicians a non-invasive three-dimensional visualization of vasculature in the retina and choroid. The visualization of perfused vasculature in a three-dimensional layout, offers clinicians an aid in the identification of retinal and choroidal pathologies such as retinal ischemia, microaneurysms, retinal neovascularization and choroidal neovascular membranes.

Non-contact white light photography

DEVICEOptical Coherence Tomography

Two and Three dimensional cross sectional imaging of the back of the eye to look at vascular structures and is an aid in the detection and management of various ocular diseases.

Sponsors

Heidelberg Engineering GmbH
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
22 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* All subjects: Able and willing to undergo the test procedures, sign informed consent, and follow instructions. * Age ≥ 22 Subjects with Normal Eyes: * Corrected visual acuity ≥ 20/40 in each eye Subjects with Pathology: * Subjects with vascular retinal conditions in at least one eye * Subjects included should have a range of retinal vascular pathologies likely to appear in OCTA imaging, affecting different anatomic depths through the retina and choroid. Retinal conditions including but not limited to diabetic retinopathy, wet age-related macular degeneration (AMD), and branch or central retinal vein occlusion that give rise to features such as retinal ischemia, microaneurysms, choroidal neovascularization and retinal neovascularization will be included.

Exclusion criteria

* All Subjects: * Subjects unable to read or write * Subjects with ocular media not sufficiently clear to obtain acceptable study- related imaging * Subjects who cannot tolerate the imaging procedures * Subjects with contraindication to pupillary dilation in the study eye * Subjects with Normal Eyes: * Subjects with uncontrolled systemic conditions, or ocular disease, as determined by the Investigator, during the eye exam and CFP * History of ocular surgical intervention (except for refractive or cataract surgery) in either eye

Design outcomes

Primary

MeasureTime frameDescription
OCTA image qualityday 1Image quality grading results of study selected images
Visualization of key anatomical vascular structures on OCTAday 1Grading of visibility of key anatomical vascular structures of study selected images

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026