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Entia Liberty: Usability Validation

NCT05027256 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 30

Last updated 2023-01-27

No results posted yet for this study

Summary

This study forms part of Entia's clinical evidence for regulatory submission. This study evaluates Entia Liberty's validation of the device. Participants will be trained to take an Entia Liberty test in a simulated home environment and a trained healthcare professional will perform another test from the same participant (different finger) on a separate device. The results will be compared. Usability data will be observed and the participants will complete a questionnaire after the tests have been performed.

Conditions

Interventions

DEVICE

Entia Liberty

Home Monitoring solution

Sponsors & Collaborators

  • Entia Ltd

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-09-12
Primary Completion
2022-11-30
Completion
2022-11-30

Countries

  • United Kingdom

Study Locations

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Entities

Diseases

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 NCT05027256 on ClinicalTrials.gov