TRK-3 Performance of Pachymetry

Completed

• Conditions: Normal
• Interventions: Device: Kerato-Refracto Tonometer

• Registration Number: NCT06250868
• Lead Sponsor: Topcon Corporation

Brief Summary

To evaluate the performance of a new tonometer.

Detailed Description

Not available

Study Timeline

• Status Verified: 2024-02
• Study First Submitted: 2024-02-01
• Study First Submitted QC: 2024-02-01
• Study First Posted: 2024-02-09
• Study Start: 2024-02-20
• Primary Completion: 2024-02-26
• Study Completion: 2024-02-26
• Last Update Submitted: 2024-02-29
• Last Update Posted: 2024-03-01

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

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

Exclusion Criteria

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

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
Normal cornea	Kerato-Refracto Tonometer	-

Primary Outcome Measures

Name	Time	Method
Cornea thickness	1 day	Thickness of the cornea

Trial Locations

Locations (1)

Topcon Healthcare Innovation Center; 🇺🇸 La Jolla, California, United States