Comparison of Intraocular Pressure Measurement With the Novel TonoVera Device With Other Commonly Used Devices
Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY
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.
Eligibility
Participation Requirements
Sex: All
Healthy Volunteers: t
View:
• 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.
Locations
United States
New York
Ross Eye Institute
RECRUITING
Buffalo
Contact Information
Primary
Sandra Sieminski, MD
smfernando17@gmail.com
716-408-6909
Backup
Catherine Seeger, MD
cseeger2@buffalo.edu
5859443719
Time Frame
Start Date: 2022-08-01
Estimated Completion Date: 2025-12-31
Participants
Target number of participants: 300
Treatments
Other: IOP Measurement
These are the measurements of the intraocular pressure.
Related Therapeutic Areas
Sponsors
Leads: State University of New York at Buffalo
Collaborators: Reichert, Inc.