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Intalight Reference Database Protocol for VG200D

NCT07751484 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 350

Last updated 2026-08-07

No results posted yet for this study

Summary

The goal of this study is to collect OCT scans on normal healthy eyes from an investigational OCT device the VG200D from Intalight, Inc, in order to establish a reference database. The reference database will be used to establish normal ranges for thickness measurement parameters provided by the VG200D OCT software including anterior segment and posterior segment measurements. The study will enroll normal eyes from three clinics in the US including a wide range of ages and races/ethnicities.

Conditions

  • The Focus of This Study is to Collect OCT Data on Normal Eyes

Interventions

DEVICE

OCT device called VG200D

This is an investigational imaging device

Sponsors & Collaborators

  • Illinois College of Optometry

    collaborator OTHER

  • Intalight, Inc

    lead INDUSTRY

Eligibility

Min Age
22 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2026-07-08
Primary Completion
2026-09-15
Completion
2026-09-15
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07751484 on ClinicalTrials.gov