[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"LumiraDx UK Limited\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":76},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,45],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":44},"100482971","collection-of-blood-samples-for-new-diagnostic-devices-2-100482971",false,"NCT05568966","Collection of Blood Samples for New Diagnostic Devices 2","Collection of Venous and Capillary Blood Samples for the Research, Optimisation and Calibration of New Diagnostic Devices 2","NOVEL-2","Inclusion Criteria\n\n* Subject 18 years of age.\n* Willing and able to provide written informed consent and comply with study procedures.\n* Patients attending a definitive care team with research capabilities which has been enroled in this collection study.\n* Patients who can read and understand written English.\n* The subject must present as one of the following cohorts:\n\n  1. Group A - Embolism Cohort - Patients presenting with symptoms indicative of thromboembolic events.\n  2. Group B - Infection or Inflammation Cohort - Patients presenting with symptoms indicative of infection or inflammatory disorders.\n  3. Group C - Cardiovascular Cohort - Patients presenting with symptoms indicative of heart failure or acute coronary syndrome.\n  4. Group D - Renal Cohort - Patients presenting with symptoms indicative of renal disorders.\n  5. Group E - Other Cohort. - Patients who are not eligible for any of the above groups.\n\nExclusion Criteria\n\n* Subject \\\u003C18 years of age.\n* Vulnerable populations deemed inappropriate for the study by the sites Principal Investigator.\n* Patients who have previously been enroled in any LumiraDx NOVEL study in the past 3 months and re-entry would breach the 24mL and or 6 fingersitck maximums.","ALL","18 Years",{"count":20,"type":21},20000,"ESTIMATED","INTERVENTIONAL",[24],"NA","To research and develop new state of the art diagnostic biomarkers on the LumiraDx Platform that are comparable to the approved gold standard reference methods and will radically enhance clinicians and patients ability to monitor health conditions and improve outcomes by delivering the results near patient at the point of care.",[27,28,29,30,31],"Embolism and Thrombosis","Cardiovascular","Renal","Inflammation","Infections","RECRUITING","2026-04-17",{"date":35,"type":36},"2026-04-22","ACTUAL",{"date":38,"type":36},"2022-07-11",{"date":40,"type":21},"2026-08-20",{"name":42,"class":43},"LumiraDx UK Limited","INDUSTRY",7,{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":50,"acronym":51,"eligibilityCriteria":52,"healthyVolunteers":11,"sex":17,"minAge":53,"maxAge":4,"enrollmentInfo":54,"targetDuration":4,"studyType":56,"phases":4,"briefSummary":57,"conditions":58,"keywords":4,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":68,"lastUpdatePostDateStruct":69,"startDateStruct":71,"completionDateStruct":73,"leadSponsor":75,"locationsCount":4},"100622045","cobas-lumira-collection-of-venous-and-capillary-blood-samples-for-the-research-optimization-and-calibration-of-new-diagnostic-devices-100622045","NCT07378514","Cobas® Lumira Collection of Venous and Capillary Blood Samples for the Research, Optimization and Calibration of New Diagnostic Devices","Cobas® Lumira Collection of Venous and Capillary Blood Samples for the Research, Optimization and Calibration of New Diagnostic Devices (EVOLVE)","EVOLVE","Inclusion Criteria:\n\n1. Willing and able to provide written informed consent.\n2. Willing to comply with study procedures.\n3. The participant must present as one of the following cohorts (primary presenting condition):\n\n   * Cohort A - Embolism Cohort (participants presenting with symptoms indicative of thromboembolic events)\n   * Cohort B - Infection or Inflammation Cohort (participants presenting with symptoms indicative of infection or inflammatory disorders)\n   * Cohort C - Cardiovascular Cohort (participants presenting with symptoms indicative of heart failure or acute coronary syndrome)\n   * Cohort D - Renal Cohort (participants presenting with symptoms indicative of renal disorders)\n   * Cohort E - Oral Anticoagulation Cohort (participants with ongoing vitamin K antagonist therapy for at least four weeks)\n   * Cohort F - Diabetes Cohort (participants with suspected pre-Diabetes or diagnosed with Diabetes Mellitus Type 1 or Type 2)\n   * Cohort G - Lipid Cohort (participants presenting with symptoms indicative for Hypercholesterolemia )\n   * Cohort H - Liver Cohort (participants with symptoms indicative of hepatic disorders).\n\nInclusion Criteria for Cohorts A, B, C, D, E, G, and H:\n\n1\\. Participants ≥ 18 years of age\n\nInclusion Criteria for Cohort F (Diabetes Cohort):\n\n1\\. Participants ≥ 16 years old\n\nExclusion Criteria:\n\n1. Subjects deemed inappropriate for the study by the Principal Investigator.\n2. Participants who have previously been enrolled in the EVOLVE study in the past 60 days.\n\nExclusion Criteria for Cohort E (Oral Anticoagulation Cohort):\n\n1. Subjects who are currently taking non-vitamin K antagonist oral anticoagulants (NOACs) including but not limited to apixaban, dabigatran etexilate, edoxaban and rivaroxaban.\n2. Subjects who have anti-phospholipid antibody syndrome (APS)\n3. 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.","16 Years",{"count":55,"type":21},30000,"OBSERVATIONAL","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.\n\nApproximately 30,000 patients are expected to participate in this study, across multiple UK sites.",[59,60,61,62,63,64,65,66],"Blood Clots","Infection and Inflammatory Reaction","Heart Disease","Kidney Disease","Vitamin K Antagonist","Diabetes","High Cholesterol","Liver Disease","NOT_YET_RECRUITING","2026-01-22",{"date":70,"type":36},"2026-01-30",{"date":72,"type":21},"2026-04",{"date":74,"type":21},"2031-07",{"name":42,"class":43},""]