TRK-3 Performance of Pachymetry

NCT ID: NCT06250868

Last Updated: 2024-03-01

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

30 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-02-20

Study Completion Date

2024-02-26

Brief Summary

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To evaluate the performance of a new tonometer.

Detailed Description

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Conditions

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Normal

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Normal cornea

Kerato-Refracto Tonometer

Intervention Type DEVICE

measures pressure inside the eye and thickness of the cornea.

Interventions

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Kerato-Refracto Tonometer

measures pressure inside the eye and thickness of the cornea.

Intervention Type DEVICE

Eligibility Criteria

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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.
Minimum Eligible Age

22 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Topcon Corporation

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Topcon Healthcare Innovation Center

La Jolla, California, United States

Site Status

Countries

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United States

Other Identifiers

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THQ-THINC-2023-03

Identifier Type: -

Identifier Source: org_study_id

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