Comparison of Intraocular Pressure Measurement With the Novel TonoVera Device With Other Commonly Used Devices
RecruitingHealthy volunteers welcome
Who can join
All ages · All sexes · Healthy volunteers welcome
Full eligibility criteria
Inclusion Criteria: * Ability to provide signed and dated informed consent form. Patients willing to comply with all study procedures and be available for the duration of the study. Male or female patients aged 18 to 99 Patients in good general health as evidenced by ability to come to their appointment on day of study. Exclusion Criteria: * Patients age less than 18 years Patients unable or unwilling to provide informed consent to participate in the study Patients for which an accurate tonometry reading cannot be performed. This may include those with blepharospasm (lid squeezers), nystagmus, extensive corneal pathology, or contact lens wearers who cannot remove their contact lens.Patients with significant scleral thinning Patients with a known allergy to proparacaine or fluorescein as these are used to anesthetize and allow measurement respectively of the eye when used with the Goldmann tonometer.
About the study
We are testing the accuracy of Reichert's Tono-Vera tonometer by comparing measurements of IOP with this device and measurements with other commonly-used tonometers, including Goldmann Applanation and iCare.
What is being tested
- Tono-Vera tonometer (device)
- Goldman Applanation Tonometry (device)
Sponsor: State University of New York at Buffalo · Participants: 300 · Started: Aug 1, 2022
Contact the study team
- Sandra Sieminski, MD · Phone: 716-408-6909
- Catherine Seeger, MD · Phone: 5859443719
Official record on ClinicalTrials.gov — NCT05523622
Locations in the U.S.
| New York | Ross Eye Institute, Buffalo |
Conditions
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.