Trials / Completed
CompletedNCT05025111
Entia Liberty: Capillary Validation
Entia Liberty: Clinical Performance Validation - Capillary Performance
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 150 (actual)
- Sponsor
- Entia Ltd · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
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
| Type | Name | Description |
|---|---|---|
| DEVICE | Entia Liberty | Home monitoring device |
Timeline
- Start date
- 2022-09-12
- Primary completion
- 2022-10-26
- Completion
- 2022-10-26
- First posted
- 2021-08-27
- Last updated
- 2023-01-27
Locations
2 sites across 1 country: United Kingdom
Source: ClinicalTrials.gov record NCT05025111. Inclusion in this directory is not an endorsement.