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Clinical Trials in the USA / NCT06920290
Active, not recruiting Observational

Visual Field Analysis With Artificial Intelligence

NCT06920290 · tracked via the Priya Life Science USA tracker
Sponsor
Sight Intelligence Engineering Corporation
Phase
Observational
Started
2025-07-01
Last updated
2025-11-03

Condition(s) studied

GlaucomaVisual Field Defect

Investigational drug(s) / intervention(s)

Visual Field Perimeter Optimized with Eye Gaze Capture and Artificial Intelligence

Visual Field Perimeter Optimized with Eye Gaze Capture and Artificial Intelligence: 1. Natural Eye Movement To the best of our knowledge, this is the first visual field perimeter software that allows users to move their eyes naturally during the test. Previous visual field tests required that patients maintain a central gaze throughout the test as test points flashed in the periphery of their vision; our test allows patients to look directly at these test points. 2. Simplified Data Capture To the best of our knowledge, this is the first visual field perimeter software that reliably eliminates the need for a hand-held clicker to register test points as the user sees them. 3. Attention Monitoring In previous tests, staring at a central spot could induce sleepiness and inattention; our test employs a software monitor that pauses the test, gives encouragement when appropriate, and allows the patient to regain focus. This allows for far greater accuracy in data reporting. 4. Artificial Intelligence (AI) Our test uses AI to optimize the test parameters.

Study summary

The purpose of this study is to analyze visual field data from healthy participants. This data will be used to develop and optimize a new visual field perimeter test. The test will incorporate an advanced algorithm, which may include the use of Artificial Intelligence (AI), to enhance accuracy and efficiency in identifying test points.

Eligibility

Sex
ALL
Min age
18 Years
Max age
100 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Healthy adults aged 18 years or older. * Best corrected visual acuity of 20/40 or better in each eye. * Normal optic nerve appearance upon clinical examination. Exclusion Criteria: * Best corrected visual acuity worse than 20/40. * Cup-to-disc ratio greater than 0.5. * Previously documented glaucoma or optic neuropathy. * Any significant ocular or neurological condition that may impact visual field. * Inability to comply with study procedures.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Sight Intelligence Engineering Alexandria Virginia

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06920290 on ClinicalTrials.gov ↗ ← All trials in the USA