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Clinical Validation of iCare IC1000 Tonometer

NCT06748092 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 168

Last updated 2026-04-07

No results posted yet for this study

Summary

Clinical validation of iCare IC1000 tonometer per ANSI Z80.10:2014 standard

Conditions

  • Intraocular Pressure

Interventions

DEVICE

iCare IC1000

Measurement of Intraocular Pressure (IOP) in sitting and supine position

DEVICE

iCare IC200

Measurement of Intraocular Pressure (IOP) in sitting and supine position

DEVICE

GAT

Measurement of Intraocular Pressure (IOP) in sitting position

DEVICE

Perkins

Measurement of Intraocular Pressure (IOP) in supine position

Sponsors & Collaborators

  • Icare Finland Oy

    lead INDUSTRY

Study Design

Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-10-21
Primary Completion
2026-03-24
Completion
2026-03-24

Countries

  • Canada

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06748092 on ClinicalTrials.gov