iCare ST500 Clinical Trial

NCT05742009 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 165

Last updated 2023-11-30

No results posted yet for this study

Summary

Clinical validation of iCare ST500 tonometer per ANSI Z80.10:2014 standard

Conditions

  • Intraocular Pressure

Interventions

DEVICE

iCare ST500

Measurement of Intraocular Pressure (IOP)

DEVICE

GAT

Measurement of Intraocular Pressure (IOP)

DEVICE

iCare IC200

Measurement of Intraocular Pressure (IOP)

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
2023-06-05
Primary Completion
2023-11-14
Completion
2023-11-14

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 NCT05742009 on ClinicalTrials.gov