TRK-3 Performance of Pachymetry | Clinical Trial

Key information

Conditions

Normal

Age range

22 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Topcon Healthcare Innovation Center

La Jolla, California, 92037, United States

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Provide voluntary written consent for participation in the study.
Age at least 22 years old at the time of informed consent.

Exclusion criteria

Ocular condition that may affect the ability to perform corneal measurement (e.g., corneal perforation, bullous keratopathy, nystagmus)
Have or is suspected to have an ocular infection in either eye.
Otherwise considered unsuitable for the study by the investigator
Unable to tolerate ophthalmic testing.

Treatment and study plan

Kerato-Refracto Tonometer

Device

measures pressure inside the eye and thickness of the cornea.

Primary outcomes

Cornea thickness

Time frame: 1 day

Thickness of the cornea

Sponsors and collaborators

Lead sponsor

Topcon Corporation

Industry

Registry information

Official study title

TRK-3 Agreement and Precision of Pachymetry Function

Important dates

Study start: 2024
Primary completion: 2024
Study completion: 2024
First posted: Feb 9, 2024
Registry last updated: Mar 1, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

Completed