Evaluation of the Repeatability and Reproducibility of OCTA Image Quality With the Heidelberg Engineering SPECTRALIS With OCT Angiography Module
Stopped early
Conditions studied: Retinal Vascular, Normal Eyes
In brief
Repeatability and Reproducibility of OCTA Image Quality with the Heidelberg Engineering SPECTRALIS
Key facts
- Study ID
- NCT03530449
- Run by
- Heidelberg Engineering GmbH
- People needed
- 39
- Starts
- 2018-04-30
- Expected to finish
- 2018-09-15
- Last updated by the study team
- 2019-02-28
Who can join
Age: 22 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- 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.
You may not qualify if…
- 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
Where it is running
- State University of New York College of Optometry (SUNY) — New York, New York, United States
Full record on ClinicalTrials.gov
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