Recruiting
Comparison of Intraocular Pressure Measurement With the Novel TonoVera Device With Other Commonly Used Devices
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.
ClinicalTrials.gov IDNCT05523622
PhaseNA
Enrollment300
SponsorState University of New York at Buffalo
AgeNo minimum reported
SexALL
Conditions studied
Glaucoma
About this 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.
Interventions
- Device: Tono-Vera tonometer — The tonometer measures intraocular pressure with a small rebound probe, similar to those used with other tonometers currently on the market, such as the iCare.
- Device: Goldman Applanation Tonometry — This is the current gold standard for measuring eye pressure.
Primary outcomes
- Intraocular Pressure (Baseline only)
Eligibility information
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.
Study locations
- Ross Eye Institute, Buffalo, New York 14209 United States
Before you participate: Varda Clinical is an independent discovery tool, not the study sponsor or a medical provider. Eligibility can only be determined by the official study team. Discuss potential risks and benefits with a qualified healthcare professional.
Source: ClinicalTrials.gov. Record last refreshed by Varda Clinical: 2026-09-27.