iCare IC1000 Alignment Study

NCT07022054 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2025-08-12

No results posted yet for this study

Summary

The primary objective of this study is to evaluate the performance of the alignment feature of iCare IC1000 tonometer.

Conditions

  • Intraocular Pressure

Interventions

DEVICE

iCare IC1000 measurement

Measurement of intraocular pressure with iCare IC1000

Sponsors & Collaborators

  • Icare Finland Oy

    lead INDUSTRY

Study Design

Allocation
NA
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-05-22
Primary Completion
2025-08-05
Completion
2025-08-05
FDA Device
Yes

Countries

  • United States

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 NCT07022054 on ClinicalTrials.gov