iCare HOME2 Clinical Trial

Status Completed

Clinical Trial Summary

The aim of this clinical study is to provide information about the variability of the intraocular pressure (IOP) self-measurements with the iCare HOME2 tonometer in comparison to the variability of the IOP measurements with the reference tonometer (iCare IC200), over a wide range of IOP values.

Clinical Trial Description

The clinical study is planned to estimate the variability of the IOP measurement of iCare HOME2 and IC200. In the study, the subjects will learn to operate the iCare HOME2 tonometer independently by using the labeling materials provided to them. Once they learn to operate the tonometer, subjects will take three self-measurements on the selected eye both in sitting and supine position. The variability of the measurement results taken with iCare HOME2 will be compared to the variability of the measurement results taken with iCare IC200 by using the recorded results from the study subjects. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05162989
Study type	Interventional
Source	Icare Finland Oy
Contact
Status	Completed
Phase	N/A
Start date	November 26, 2021
Completion date	December 15, 2021

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