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Performance Evaluation of DIY Digital Visual Acuity Test

NCT07331870 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 70

Last updated 2026-01-12

No results posted yet for this study

Summary

This study aims to verify the accuracy of a new Digital Visual Acuity test. The test results obtained with the support of the device will be compared to the current standard of care related to visual acuity testing.

Conditions

  • Visual Acuity

Interventions

DEVICE

Comparaison of the investigation device measurement with standard of Care

The patient Visual acuity is measured with the investigational device, the ETDRS method, the radner test and the results are compared.

Sponsors & Collaborators

  • Veranex Switzerland SA

    collaborator INDUSTRY

  • Ojenforeningen

    lead OTHER

Principal Investigators

  • Lisbeth Sandfeld, PhD MD · Zealand University Hospital, Roskilde, Denmark

Study Design

Allocation
NA
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-10-01
Primary Completion
2025-11-15
Completion
2025-11-15

Countries

  • Denmark

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 NCT07331870 on ClinicalTrials.gov