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Entia Liberty: Capillary Validation

NCT05025111 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 150

Last updated 2023-01-27

No results posted yet for this study

Summary

This study is a clinical performance validation study to evaluate the performance of the Entia Liberty device. Patients undergoing routine venepuncture blood tests will be recruited to have an Entia Liberty test (by finger-prick) done on them by a trained healthcare professional. The results from that finger-prick test will be compared against the results from the routine venepuncture blood test (reference method) and subsequently, excess blood from the routine venepuncture test will be run on another Entia Liberty device in the laboratory. All three results (Entia Liberty capillary, Entia Liberty venous and gold standard venous) will be compared against each other to prove Entia Liberty's performance claims.

Conditions

Interventions

DEVICE

Entia Liberty

Home monitoring device

Sponsors & Collaborators

  • The Christie NHS Foundation Trust

    collaborator OTHER

  • Entia Ltd

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-09-12
Primary Completion
2022-10-26
Completion
2022-10-26

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 NCT05025111 on ClinicalTrials.gov