Icare Tonometry Effects on Keratometry Readings, Topography Readings, and Corneal Staining

NACompletedINTERVENTIONAL
Enrollment

60

Participants

Timeline

Start Date

June 19, 2017

Primary Completion Date

July 31, 2018

Study Completion Date

July 31, 2018

Conditions
Evaluation of Corneal Stability Post-applanation
Interventions
DEVICE

Icare tonometer

Icare tonometry effects of keratometry readings, topography, and corneal staining to demonstrate that the Icare tonometer does not alter subsequent evaluation or testing. This would allow IOP testing to be performed by technical staff at any time during the examination process without affecting subsequent tests. A total of fifteen patients at each of four sites will be evaluated using Icare tonometers provided by Icare USA. The investigator will be masked as to which eye will undergo Icare tonometry. Both the study eye and the control eye will undergo pre-tonometry and post-tonometry testing; Keratometry readings, IOL master, Topography via Pentacam, and corneal staining with fluorescein using the Oxford scoring scale.

Trial Locations (1)

43082

Comprehensive EyeCare of Central Ohio, Westerville

All Listed Sponsors
collaborator

Icare USA

UNKNOWN

lead

Comprehensive EyeCare of Central Ohio

OTHER

NCT03275142 - Icare Tonometry Effects on Keratometry Readings, Topography Readings, and Corneal Staining | Biotech Hunter | Biotech Hunter