Clinical Trials Directory

Trials / Completed

CompletedNCT01159340

Icare Versus Haag-Streit Applanation Tonometer

Design Compliance Testing of the Icare One Rebound Tonometer According to the American National Standard ANSI Z80.10-2001 and International Standard ISO 8612.2 for Tonometers

Status
Completed
Phase
Study type
Observational
Enrollment
260 (actual)
Sponsor
Icare Finland Oy · Industry
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

The clinical performance of Icare ONE Tonometer TA02 was compared to a Goldmann type applanation tonometer (Haag-Streit). Data was collected according to ANSI Z80.10-2003 (ISO 8612.2) standard. Subjects were eligible for the study if they had no exclusion criteria specified in the ANSI/ISO standard. One eye from 260 subjects was selected for the study. The minimum sample size according to the standard is 150. One eye of each subject was selected for the study by an investigator, based on the history of the patient, results of an external examination of the eye with slit lamp, keratometry readings, and prior knowledge of the intraocular pressure (IOP) range. The Icare ONE Tonometer TA02 in comparison to the reference tonometer (Goldmann type tonometer).

Conditions

Timeline

Start date
2009-05-01
Completion
2009-11-01
First posted
2010-07-09
Last updated
2010-07-09

Locations

1 site across 1 country: Finland

Source: ClinicalTrials.gov record NCT01159340. Inclusion in this directory is not an endorsement.