Skip to content
Trial Eligibility
Menu

Intalight Reference Database Protocol for VG200D

NCT07751484

This study is recruiting at 3 US sites in 3 states, according to its ClinicalTrials.gov record last updated .

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.

Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov

Conditions studied

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

Eligibility basics and study details

Study type
Observational
Phase
Not applicable
Ages
22 years and older
Sex
All
Healthy volunteers
Accepted
Sponsor
Intalight, Inc
Last updated on ClinicalTrials.gov
August 7, 2026

These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.

US recruiting sites

California · 1

  • New View Optometry · San Diego, CA

Illinois · 1

  • Illinois College of Optometry · Chicago, IL

Indiana · 1

  • Indiana University - School of Optometry · Bloomington, IN

Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.