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.