Comparative Study of the NIDEK TONOREF III With Predicate Devices

Status Not yet recruiting

Clinical Trial Summary

The primary objective of this clinical study is to prove that tonometry values for NIDEK TONOREF III are comparable to the predicate device and to prove that the pachymeter function of NIDEK TONOREF III is equivalent to the predicate device. The secondary objective is to demonstrate that the test device is as safe as the predicate devices.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Intraocular Pressure

Clinical Trial Details

NCT number	NCT06363045
Study type	Interventional
Source	Nidek Co. LTD.
Contact	Tadakazu Ichimura
Phone	0533678904
Email	tadakazu_ichimura@nidek.co.jp
Status	Not yet recruiting
Phase	N/A
Start date	May 2024
Completion date	November 2024

View Details

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