Recruiting

OCT Scans

Sponsor:

Intalight, Inc

Code:

NCT07751484

Conditions

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

Eligibility Criteria

Sex: All

Age: 22+

Healthy Volunteers: Accepted

Interventions

OCT device called VG200D

Study Details

Brief 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

Study ID

NCT07751484

Start date

Jul 8, 2026

Status verified date

Aug, 2026

Completion date

Sep 15, 2026

Anticipated

Primary completion date

Sep 15, 2026

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 22+

Healthy Volunteers: Accepted

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.

4\. 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

Study Design

Enrollment

350 participants

Anticipated

Interventions and Outcome Measures

Arms

Normal

This group includes subjects with normal healthy eyes as confirmed by a clinical examination by trained eye-care professionals

Interventions

OCT device called VG200D

This is an investigational imaging device

Primary outcome measure

  • Quantitative ocular structures [ Time Frame: this study will alst approximately 6 months ]

Central Contacts and Locations

Central contacts

Mike Sinai, PhD

6198067636mike.sinai@gmail.com

Locations

New View Optometry

Recruiting

San Diego, California, United States, 91942

Contacts

David Kasanoff, OD

619-465-7900davksnf@gmail.com

Principal Investigator:

David Kasanoff, OD

Illinois College of Optometry

Recruiting

Chicago, Illinois, United States, 60616

Contacts

Michael Chaglasian, OD

312-949-7000mchaglas@ico.edu

Principal Investigator:

Michael Chaglasian, OD

Indiana University - School of Optometry

Recruiting

Bloomington, Indiana, United States, 47405

Contacts

Brett King, OD

812-855-4447kingbrj@iu.edu

Principal Investigator:

Brett King, OD

More Information

Sponsor

Intalight, Inc

Last update posted

Aug 7, 2026

Last verified

Aug, 2026

Keywords

  • Optical Coherence Tomography

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-09. This information was provided to ClinicalTrials.gov by Intalight, Inc on 2026-08-07.