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TRK-3 Performance of Pachymetry

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Status

Completed

Conditions

Normal

Treatments

Device: Kerato-Refracto Tonometer

Study type

Observational

Funder types

Industry

Identifiers

NCT06250868
THQ-THINC-2023-03

Details and patient eligibility

About

To evaluate the performance of a new tonometer.

Enrollment

30 patients

Sex

All

Ages

22+ years old

Volunteers

Accepts Healthy Volunteers

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.

Trial design

30 participants in 1 patient group

Normal cornea
Treatment:
Device: Kerato-Refracto Tonometer

Trial contacts and locations

1

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Central trial contact

Mayra Study Coordinator

Data sourced from clinicaltrials.gov

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