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RECRUITING NA

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

NCT07449195 · View on ClinicalTrials.gov ↗

Study 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

Conditions Studied

Interventions

  • DIAGNOSTIC_TEST Intalight Dream OCT
  • DIAGNOSTIC_TEST Heidelberg Spectralis OCT

Study Locations (7)

New York

  • Memorial Sloan Kettering Cancer Center @ Suffolk-Commack (Consent only) — Commack
  • Memorial Sloan Kettering Westchester (Consent Only) — Harrison
  • Memorial Sloan Kettering Cancer Center (All Protocol Activites) — New York
  • Memorial Sloan Kettering Cancer Center @ Nassau (Consent only) — Uniondale

New Jersey

  • Memorial Sloan Kettering at Basking Ridge (Consent Only) — Basking Ridge
  • Memorial Sloan Kettering Monmouth (Consent only) — Middletown
  • Memorial Sloan Kettering Bergen (Consent Only) — Montvale

Trial Details

FieldValue
Enrollment Target 60 participants
Start Date 2026-02-27
Est. Completion 2028-02-27
Phase NA

Sponsor

Memorial Sloan Kettering Cancer Center

2,280 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT07449195

The ClinicalTrials.gov registry entry for NCT07449195 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 60 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Memorial Sloan Kettering Cancer Center, which has 2,280 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Ocular Tumor appearing as the primary indexed condition, and to 2 interventions — of which Intalight Dream OCT is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT07449195 reports 7 study locations spanning 2 distinct geographic areas — top geographies include New York, New Jersey. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT07449195 about?

NCT07449195 is a clinical study titled "A Study Comparing Two Optical Coherence Tomography Devices in People With Ocular Tumors". 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

What is the current status of trial NCT07449195?

This trial is currently recruiting. It is a NA study. The enrollment target is 60 participants. The study started on 2026-02-27. Estimated completion is 2028-02-27.

What conditions does trial NCT07449195 study?

This clinical trial studies the following conditions: Ocular Tumor. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT07449195?

The interventions under investigation include: Intalight Dream OCT (DIAGNOSTIC_TEST), Heidelberg Spectralis OCT (DIAGNOSTIC_TEST). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT07449195?

This trial is sponsored by Memorial Sloan Kettering Cancer Center, which has 2,280 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT07449195 being conducted?

This trial has 7 study locations across New Jersey, New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial