A Study Comparing Two Optical Coherence Tomography Devices in People With Ocular Tumors

ConditionOcular Tumor
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorMemorial Sloan Kettering Cancer Center

About this trial

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 criteria

This trial does not accept healthy volunteers

Qualifiers

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.

Disqualifiers

Does not meet ALL of the above conditions

Trial design

Design model

Single group

Treatments tested in this trial

  • Intalight Dream OCT

    Diagnostic test

    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.

  • Heidelberg Spectralis OCT

    Diagnostic test

    This is the standard of care for optical imaging.

Treatment groups

60 Participants
are divided into 1 treatment group
Group A: Participants with Ocular TumorExperimental treatment 2 interventions

Trial outcomes

Primary outcomes

1

Image quality for participants

Evaluated by next-generation swept-source OCT versus standard OCT for imaging of the eye and any relevant ocular tumors.

Time frame
Up to 1 year
2

Field of view for participants

Evaluated by next-generation swept-source OCT versus standard OCT for imaging of the eye and any relevant ocular tumors.

Time frame
Up to 1 year

Secondary outcomes

Other outcomes

Sponsors and contacts

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