Clinical Trials Directory

Trials / Completed

CompletedNCT06363045

Comparative Study of the NIDEK TONOREF III with Predicate Devices

Comparative Study of the NIDEK TONOREF III with the Haag-Streit, Perkins Hand-held Applanation Tonometer for Tonometry Function and NIDEK TONOREF III with the NIDEK CEM-530 for Pachymetry Function

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
183 (actual)
Sponsor
Nidek Co. LTD. · Industry
Sex
All
Age
18 Years
Healthy volunteers
Accepted

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.

Conditions

Interventions

TypeNameDescription
DEVICENIDEK TONOREF IIIThe auto ref/kerato/tono/pachymeter TONOREF III is a medical device which measures objective refractive errors, corneal curvature radius, intraocular pressure and corneal thickness of the patient's eye.
DEVICEHaag-Streit, PERKINS HAND-HELD APPLANATION TONOMETERHaag-Streit Goldmann Manual Tonometer measures intraocular pressure to aid in the screening and diagnosis of glaucoma
DEVICENIDEK CEM-530Nidek CEM-530 is a non-contact ophthalmic microscope, optical pachymeter, and camera used for examination of the corneal endothelium and for measurement of the thickness of the cornea.

Timeline

Start date
2024-06-27
Primary completion
2024-12-13
Completion
2024-12-13
First posted
2024-04-12
Last updated
2025-03-07

Locations

1 site across 1 country: United Kingdom

Source: ClinicalTrials.gov record NCT06363045. Inclusion in this directory is not an endorsement.