A Study Comparing Two Optical Coherence Tomography Devices in People With Ocular Tumors
Ocular Imaging for Monitoring of Ocular Tumor Disease
Memorial Sloan Kettering Cancer Center
60 participants
Feb 27, 2026
INTERVENTIONAL
Conditions
Summary
The purpose of this study is to compare two devices used for optical coherence tomography (OCT). OCT is a noninvasive imaging (scanning) method that uses reflected light to create pictures of the back of the eye, and doctors can use OCT to detect and monitor different types of cancer
Eligibility
Inclusion Criteria7
- Age ≥18 years.
- At least 1 eye that has an intraocular or ocular surface tumor.
- The presence of a natural crystalline lens or intraocular lens.
- Pupils that can dilate up to at least 3 mm in the study eyes.
- The absence of opaque natural crystalline lenses or the presence of any ocular disease that prevents the view of the retina for imaging.
- Patients must be able to fixate on the imaging target.
- Patients must be able to sit still for a period of time (approximately 2 minutes).
Exclusion Criteria1
- Does not meet ALL of the above conditions
Interested in this trial?
Get notified about updates and connect with the research team.
Interventions
This is a next-generation swept-source device that has a faster imaging speed and higher sensitivity than the previous generation of frequency-domain OCT devices, which serve as the current standard of care devices.
This is the standard of care for optical imaging.
Locations(7)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT07449195