[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"blood-pressure-measurement\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:blood-pressure-measurement":24},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,42,66,80],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":15,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":4,"briefSummary":22,"conditions":23,"keywords":25,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":30,"lastUpdatePostDateStruct":31,"startDateStruct":34,"completionDateStruct":36,"leadSponsor":38,"locationsCount":41},"100649823","blood-pressure-measurement-using-vitacam-100649823",false,"NCT07739667","Blood Pressure Measurement Using Vitacam","Inclusion Criteria:\n\n* Age 18 years or older\n* Ability to give informed consent\n* Volunteering for the study\n* Fluent Finnish or English\n\nExclusion Criteria:\n\n* Age under 18 years\n* Pregnancy\n* Inability to give informed consent\n* Denial",true,"ALL","18 Years",{"count":19,"type":20},85,"ESTIMATED","OBSERVATIONAL","The purpose of this clinical investigation is to collect data for the development, testing, and validation of a blood pressure measurement algorithm for a contactless vital signs monitor, Vitacam, according to the ISO 80601-2:2019 standard for validating non-invasive sphygmomanometer, with the intention of disseminating the validation results through a peer-reviewed scientific publication.",[24],"Blood Pressure Measurement",[26,27,28],"blood pressure","remote photoplethysmography","rppg","RECRUITING","2026-07-28",{"date":32,"type":33},"2026-07-31","ACTUAL",{"date":35,"type":33},"2026-05-11",{"date":37,"type":20},"2027-03-31",{"name":39,"class":40},"Evondos Oy","INDUSTRY",1,{"id":43,"slug":44,"hasResults":11,"nctId":45,"briefTitle":46,"officialTitle":47,"acronym":4,"eligibilityCriteria":48,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":49,"targetDuration":4,"studyType":51,"phases":52,"briefSummary":54,"conditions":55,"keywords":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":57,"lastUpdatePostDateStruct":58,"startDateStruct":60,"completionDateStruct":62,"leadSponsor":64,"locationsCount":41},"100645954","nibp-accuracy-study-for-adult-subject-populations-100645954","NCT07697950","NIBP Accuracy Study for Adult Subject Populations","Non-Invasive Blood Pressure Accuracy Study for Adult Subject Populations","Inclusion Criteria:\n\n1. Age requirement: 18 and over.\n2. Have an upper limb (right OR left side) that fits the cuff size of the device (circumference ranging 17 cm to 40 cm) OR have a thigh (right OR left side) that fits a cuff size of the device (circumference ranging 38 to 50 cm).\n3. Have an arterial line as a standard of care, which measures blood pressure at the aortic root.\n4. Able to provide written informed consent.\n5. Expected to remain in the unit for the duration of the study procedure.\n\nExclusion Criteria:\n\n1. Have previously participated in this study (no subject may participate more than once).\n2. Pregnant and lactating women per site standard of care.\n3. Subjects with peripheral arterial diseases (causing left\u002Fright arm difference)\n4. Hemodynamically unstable subjects at the discretion of the investigator.\n5. Exhibited injuries, deformities, intravenous lines, or other abnormalities that, in the opinion of the Investigator, may prevent proper cuff application or functioning.\n6. Are suffering from infection(s) or immunocompromised patients that require isolation.\n7. PI or designee decision due to subject health conditions",{"count":50,"type":20},130,"INTERVENTIONAL",[53],"NA","The purpose of this study is to collect NIBP and invasive aortic pressure data from the clinical setting.",[24,56],"Blood Pressure","2026-07-07",{"date":59,"type":33},"2026-07-13",{"date":61,"type":33},"2025-01-13",{"date":63,"type":20},"2027-12-31",{"name":65,"class":40},"GE Healthcare",{"id":67,"slug":68,"hasResults":11,"nctId":69,"briefTitle":47,"officialTitle":47,"acronym":4,"eligibilityCriteria":48,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":70,"targetDuration":4,"studyType":51,"phases":71,"briefSummary":54,"conditions":72,"keywords":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":57,"lastUpdatePostDateStruct":73,"startDateStruct":75,"completionDateStruct":77,"leadSponsor":79,"locationsCount":41},"100643127","non-invasive-blood-pressure-accuracy-study-for-adult-subject-populations-100643127","NCT07628296",{"count":50,"type":20},[53],[56,24],{"date":74,"type":33},"2026-07-08",{"date":76,"type":33},"2026-05-19",{"date":78,"type":20},"2027-06-30",{"name":65,"class":40},{"id":81,"slug":82,"hasResults":11,"nctId":83,"briefTitle":84,"officialTitle":85,"acronym":4,"eligibilityCriteria":86,"healthyVolunteers":11,"sex":16,"minAge":4,"maxAge":17,"enrollmentInfo":87,"targetDuration":4,"studyType":51,"phases":89,"briefSummary":90,"conditions":91,"keywords":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":92,"lastUpdatePostDateStruct":93,"startDateStruct":95,"completionDateStruct":97,"leadSponsor":99,"locationsCount":100},"100646970","nibp-study-for-neonate-and-pediatric-subject-populations-100646970","NCT07684885","NIBP Study for Neonate and Pediatric Subject Populations","Non-Invasive Blood Pressure Accuracy Study for Neonate and Pediatric Subject Populations","Inclusion Criteria:\n\n* Age requirement: 0 to \\\u003C 18 years.\n* For children under 15 years old: Has a guardian or other legal representative who is able to provide consent of a guardian OR\n* For children between the age of 15-17 years; able to provide written consent form and the legal guardians can be reached to be informed of the study participation.\n* Have an upper limb (right OR left side) that fits the cuff size of the device (circumference ranging 3 cm to 33 cm) OR have a thigh (right OR left side) that fits a cuff size of the device (circumference ranging 38 to 50 cm).\n* Have an arterial line as a standard of care, which measures invasive blood pressure.\n* Expected to remain in the unit for the duration of the study procedure.\n\nExclusion Criteria:\n\n* Have previously participated in this study (no subject may participate more than once).\n* Subjects with peripheral arterial diseases (causing left\u002Fright arm difference).\n* Hemodynamically unstable subjects Subjects with complications on vasoactive agents at discretion of the Investigator.\n* Exhibited injuries, deformities, intravenous lines, or other abnormalities that, in the opinion of the Investigator, may prevent proper cuff application or functioning.\n* Are suffering from infection(s) or immunocompromised subjects that require isolation.\n* For adolescents of child-bearing potential, who are currently pregnant, suspected to be pregnant, or are currently lactating.\n* PI, designee or caring physician decision due to subject health conditions",{"count":88,"type":20},110,[53],"The purpose of this study is developing new NIBP enhancement and test it in clinical environment with neonates and children population subjects.",[56,24],"2026-06-29",{"date":94,"type":33},"2026-07-06",{"date":96,"type":33},"2025-05-14",{"date":98,"type":20},"2026-12-31",{"name":65,"class":40},2]