MedTrace Logo

Intraocular Pressure Data Collection With Tonometers

NCT06450587 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 151

Last updated 2025-04-30

No results posted yet for this study

Summary

The goal of this clinical trial is to collect a comprehensive dataset of intraocular pressure values for developing a measurement algorithm for the new hand-held rebound tonometer device. The measurement algorithm shall fulfill the requirements of ANSI Z80.10:2014 standard. The study population is adults (age ≥ 18 years).

The intraocular pressure of the participants will be measured with four different tonometers.

Conditions

  • Intraocular Pressure

Interventions

DEVICE

iCare IC1000

Measurement of Intraocular Pressure (IOP)

DEVICE

iCare ST500

Measurement of Intraocular Pressure (IOP)

DEVICE

iCare IC200

Measurement of Intraocular Pressure (IOP)

DEVICE

GAT

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
2024-05-29
Primary Completion
2025-02-07
Completion
2025-02-07

Countries

  • Slovenia

Study Locations

More Related Trials

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 NCT06450587 on ClinicalTrials.gov