Clinical Study of the Topcon Pachymeter TRK-3 to Evaluate Agreement and Precision

NCT05283343 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 30

Last updated 2022-07-22

No results posted yet for this study

Summary

Agreement and Precision of corneal thickness measurement (pachymetry) function of the test device TRK-3 and the predicate device SP-1P will be evaluated in volunteers, and safety will be evaluated.

Conditions

  • Corneal Thickness

Interventions

DEVICE

SP-1P

A subject undergoes corneal thickness measurement with pachymeter.

Sponsors & Collaborators

  • Topcon Corporation

    lead INDUSTRY

Eligibility

Min Age
20 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-11-27
Primary Completion
2021-11-27
Completion
2021-11-27

Countries

  • Japan

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05283343 on ClinicalTrials.gov