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Intalight Reference Database Protocol for VG200D

Intalight, Inc · with Illinois College of Optometry · NCT07751484

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Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.

Key facts

Compensation
Not posted. Ask the study team before screening.
Who can join
Ages 22+ · All sexes
Healthy volunteers
Accepted
Study type
Observational
Target enrollment
350
US sites recruiting
3
Study start
July 8, 2026
Record last updated
August 7, 2026

Status re-checked against ClinicalTrials.gov within the last 12 hours.

What the study is about

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.

Being studied: OCT device called VG200D

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

Eligibility criteria

Copied from the official record. The study team makes the final decision at screening.

Show full criteria

Inclusion Criteria

  • 1. Subject 22 years of age or older on the date of informed consent 2. Subject able to understand the written informed consent and willing to participate as evidenced by signing the informed consent 3. Subjects presenting at the site with normal eyes. Cataracts, LASIK, PRK, and peripheral pathology that does not affect the posterior pole region, for example lattice and peripheral drusen, are allowed.
  • BCVA 20/40 or better (each eye) 5. Subject is able to comply with the study procedures

Exclusion Criteria

  • 1. Subject unable to tolerate ophthalmic imaging 2. Subject has an ocular pathology other than cataract or mild peripheral, age-related changes (e.g., peripheral drusen, lattice, etc.) 3. Glaucoma diagnosis in either eye. 4. Subject has a condition or is in a situation which the investigator feels may put the subject at significant risk, may confound the study results, or may interfere significantly with the subject's participation in the study 5. Subject with ocular media not sufficiently clear to obtain acceptable OCT images

Recruiting US locations

  • New View Optometry

    San Diego, CA 91942

    Site contact: David Kasanoff, OD · 619-465-7900 · davksnf@gmail.com

  • Illinois College of Optometry

    Chicago, IL 60616

    Site contact: Michael Chaglasian, OD · 312-949-7000 · mchaglas@ico.edu

  • Indiana University - School of Optometry

    Bloomington, IN 47405

    Site contact: Brett King, OD · 812-855-4447 · kingbrj@iu.edu

Study contacts (from the official record)

  • Mike Sinai, PhD · 6198067636 · mike.sinai@gmail.com
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Intalight Reference Database Protocol for VG200D (NCT07751484) | Bored Studies