[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"renal\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:renal":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"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]