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NCT07378514

Cobas® Lumira Collection of Venous and Capillary Blood Samples for the Research, Optimization and Calibration of New Diagnostic Devices

Sponsor: LumiraDx UK Limited

View on ClinicalTrials.gov

Summary

This study is a blood sample collection study, collecting venous and capillary blood samples from adult patients in the UK, with a range of health conditions. The purpose of this study is to collect blood samples to help develop, improve, and fine-tune new and existing diagnostic tests for the cobas® lumira instrument. This instrument is a diagnostic medical device with single-use test strips, that allows diagnostic testing right at the patient's side. The aim is to improve doctors' ability to monitor health conditions more quickly and easily. Approximately 30,000 patients are expected to participate in this study, across multiple UK sites.

Official title: Cobas® Lumira Collection of Venous and Capillary Blood Samples for the Research, Optimization and Calibration of New Diagnostic Devices (EVOLVE)

Key Details

Gender

All

Age Range

16 Years - Any

Study Type

OBSERVATIONAL

Enrollment

30000

Start Date

2026-04

Completion Date

2031-07

Last Updated

2026-01-30

Healthy Volunteers

Conditions

Blood Clots Infection and Inflammatory Reaction Heart Disease Kidney Disease Vitamin K Antagonist Diabetes High Cholesterol Liver Disease

Interventions

DIAGNOSTIC_TEST

Blood samples are obtained and pseudonymized, prior to use for the development, optimization and calibration of diagnostic tests

Inclusion Criteria: 1. Willing and able to provide written informed consent. 2. Willing to comply with study procedures. 3. The participant must present as one of the following cohorts (primary presenting condition): * Cohort A - Embolism Cohort (participants presenting with symptoms indicative of thromboembolic events) * Cohort B - Infection or Inflammation Cohort (participants presenting with symptoms indicative of infection or inflammatory disorders) * Cohort C - Cardiovascular Cohort (participants presenting with symptoms indicative of heart failure or acute coronary syndrome) * Cohort D - Renal Cohort (participants presenting with symptoms indicative of renal disorders) * Cohort E - Oral Anticoagulation Cohort (participants with ongoing vitamin K antagonist therapy for at least four weeks) * Cohort F - Diabetes Cohort (participants with suspected pre-Diabetes or diagnosed with Diabetes Mellitus Type 1 or Type 2) * Cohort G - Lipid Cohort (participants presenting with symptoms indicative for Hypercholesterolemia ) * Cohort H - Liver Cohort (participants with symptoms indicative of hepatic disorders). Inclusion Criteria for Cohorts A, B, C, D, E, G, and H: 1\. Participants ≥ 18 years of age Inclusion Criteria for Cohort F (Diabetes Cohort): 1\. Participants ≥ 16 years old Exclusion Criteria: 1. Subjects deemed inappropriate for the study by the Principal Investigator. 2. Participants who have previously been enrolled in the EVOLVE study in the past 60 days. Exclusion Criteria for Cohort E (Oral Anticoagulation Cohort): 1. Subjects who are currently taking non-vitamin K antagonist oral anticoagulants (NOACs) including but not limited to apixaban, dabigatran etexilate, edoxaban and rivaroxaban. 2. Subjects who have anti-phospholipid antibody syndrome (APS) 3. The participant is currently receiving or has received within the past thirty (30) days of the study visit an experimental biologic, experimental drug, or experimental device including either treatment or therapy.