RecruitingNot ApplicableNCT07680244

(CIRRUS-2023-1) CLINICAL CLIN Assessment of PathFinder 1.0 on the CIRRUS 6000 and the CIRRUS 5000


Sponsor

Carl Zeiss Meditec-Dublin CoCe

Enrollment

400 participants

Start Date

May 23, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

This study will measure how well PathFinder 1.0 detects retinal abnormalities on macular cube OCT B-scans by assessing its sensitivity and specificity.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a medical device called PathFinder 1.0 on CIRRUS HD-OCT for people with dry age-related macular degeneration, epiretinal membrane, and other related conditions. The study is currently recruiting participants at 6 locations. People eligible for this study include aged 18 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DEVICEPathFinder 1.0 on CIRRUS HD-OCT

Participants undergo standard OCT imaging on CIRRUS HD-OCT systems, and the investigational PathFinder software analyzes the images for macular abnormalities without influencing clinical care.


Locations(6)

Retina Associates

Tucson, Arizona, United States

Northern California Retina Vitreous Associates

Mountain View, California, United States

Premier Eyecare of San Francisco

San Francisco, California, United States

Nova Southeastern University College of Optometry

Fort Lauderdale, Florida, United States

Eyecare Medical Group

Portland, Maine, United States

Moyes Eye Center

Kansas City, Missouri, United States

View Full Details on ClinicalTrials.gov

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NCT07680244


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