iCare vs Tonopen vs Goldmann Applanation Post-vitrectomy Surgery

Status Completed

Clinical Trial Summary

The purpose of the study is to compare the measurement of pressure inside the eye using three different FDA-approved devices (Icare, Tonopen, and Goldmann applanation).

Clinical Trial Description

The three above devices will be used to measure intraocular pressure in patients one day following vitreoretinal surgery. The underlying reason for surgery is not being considered in this study. The measured pressures will be compared across devices in eyes filled with fluid, gas, and silicone oil. ;

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic

Related Conditions & MeSH terms

Intraocular Pressure

Clinical Trial Details

NCT number	NCT01786954
Study type	Interventional
Source	Duke University
Contact
Status	Completed
Phase	N/A
Start date	October 2012
Completion date	September 2014

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