[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100569768":3},{"organization":4,"outcomesModule":7,"designInfo":14,"detailedDescription":13,"studyPopulation":13,"armGroups":21,"interventions":27,"overallOfficials":13,"centralContacts":32,"locations":38,"responsibleParty":57,"collaborators":13,"id":59,"slug":13,"hasResults":60,"nctId":61,"briefTitle":62,"officialTitle":63,"acronym":64,"eligibilityCriteria":65,"healthyVolunteers":66,"sex":67,"minAge":68,"maxAge":69,"enrollmentInfo":70,"targetDuration":13,"studyType":73,"phases":74,"briefSummary":75,"conditions":76,"keywords":78,"overallStatus":41,"whyStopped":13,"lastUpdateSubmitDate":81,"lastUpdatePostDateStruct":82,"startDateStruct":85,"completionDateStruct":87,"leadSponsor":89,"locationsCount":90},{"fullName":5,"class":6},"Aktiia SA","INDUSTRY",{"primaryOutcomes":8,"secondaryOutcomes":13,"otherOutcomes":13},[9],{"measure":10,"description":11,"timeFrame":12},"Data set build","Number of subjects including three assessments of blood pressure using Aktiia G2C Clinical, alongside three assessments of blood pressure with Aktiia Bracelet G2 and three values of blood pressure generated with the Aktiia Init I1 oscillometric cuff","Baseline",null,{"allocation":15,"interventionModel":16,"interventionModelDescription":17,"primaryPurpose":18,"observationalModel":13,"timePerspective":13,"maskingInfo":19},"NA","SINGLE_GROUP","Study subjects are asked to stay seated while 3 successive measurements are taken with the device under investigation (BP and PR) and two references (Aktiia Bracelet G2 and Aktiia Init I1 oscillometric cuff).","OTHER",{"masking":20,"maskingDescription":13,"whoMasked":13},"NONE",[22],{"label":23,"type":18,"description":24,"interventionNames":25},"Aktiia G2C cohort","Study subjects are asked to stay seated while 3 successive measurements are taken with the Aktiia G2C device under investigation (BP and PR) and two references (Aktiia Bracelet G2 and Aktiia Init I1 oscillometric cuff).",[26],"Device: Aktiia G2C",[28],{"type":29,"name":30,"description":24,"armGroupLabels":31,"otherNames":13},"DEVICE","Aktiia G2C",[23],[33],{"name":34,"role":35,"phone":36,"phoneExt":13,"email":37},"Pascale Vermare","CONTACT","+41 32 552 20 52","pascale.vermare@aktiia.com",[39],{"facility":40,"status":41,"city":42,"state":13,"zip":43,"country":44,"countryCode":45,"cosmosGeoPoint":46,"geoPoint":51,"contacts":52},"CHUV Service de Néphrologie et d'Hypertension","RECRUITING","Lausanne","1011","Switzerland","CH",{"type":47,"coordinates":48},"Point",[49,50],6.63282,46.516,{"lat":50,"lon":49},[53],{"name":54,"role":35,"phone":55,"phoneExt":13,"email":56},"Grégoire WUERZNER, Prof. Med.","+41 21 314 02 23","gregoire.wuerzner@chuv.ch",{"type":58,"investigatorFullName":13,"investigatorTitle":13,"investigatorAffiliation":13,"oldNameTitle":13,"oldOrganization":13},"SPONSOR","100569768",false,"NCT06698536","OBPM_COYOTE2024 Physiological Data Recording With the Calibration-free Optical Aktiia G2C Device at Fingertip and Wrist, Alongside the Aktiia Oscillometric Cuff","OBPM_COYOTE2024 Physiological Data Recording With the Calibration-free Optical Aktiia G2C Device at Fingertip and Wrist, Alongside the Aktiia Oscillometric Cuff: a Single-center, Prospective Clinical Study","COYOTE2024","Inclusion Criteria:\n\n* Subjects aged 21 to 85yo\n* Subjects or witnesses fluent in written and spoken French\n* Subjects agreeing to attend the study visit and follow study procedures\n* Subjects that have signed the informed consent form.\n\nExclusion Criteria:\n\n* Amputated index fingers\n* Damaged\u002Finjured skin at index fingers\n* Damaged\u002Finjured skin at wrists\n* Subjects with tachycardia (heart rate at rest \\> 120bpm)\n* Subjects with atrial fibrillation\n* Subjects with diabetes\n* Subjects with marked renal dysfunctions (eGFR \\\u003C 30mL\u002Fmin\u002F1.73 m2)\n* Subjects with untreated hyper-\u002Fhypothyroidism\n* Subjects with pheochromocytoma\n* Subjects with Raynaud's disease\n* Subjects with an arteriovenous fistula\n* Women in known pregnancy\n* History of polyneuropathy",true,"ALL","21 Years","85 Years",{"count":71,"type":72},255,"ESTIMATED","INTERVENTIONAL",[15],"The present study, OBPM\\_COYOTE2024, with N = 255 participants minimum over 1 visit (lasting \\~15min), has been designed to collect raw optical data with Aktiia.product-G2C Clinical investigational device together with Aktiia G2 Bracelet and Aktiia Init I1 oscillometric cuff within a cohort of subjects characterized by a wide variety of phenotypes. The resulting dataset will support research and development activities conducted by AKTIIA SA out of the study context.",[77],"Hypertension",[79,80],"hypertension","blood pressure","2025-05-12",{"date":83,"type":84},"2025-05-14","ACTUAL",{"date":86,"type":84},"2024-12-20",{"date":88,"type":72},"2026-12-31",{"name":5,"class":6},1]