[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100418049":3},{"organization":4,"armGroups":7,"interventions":18,"overallOfficials":10,"centralContacts":24,"locations":33,"responsibleParty":56,"collaborators":10,"id":60,"slug":10,"hasResults":61,"nctId":62,"briefTitle":63,"officialTitle":64,"acronym":10,"eligibilityCriteria":65,"healthyVolunteers":66,"sex":67,"minAge":10,"maxAge":68,"enrollmentInfo":69,"targetDuration":10,"studyType":72,"phases":10,"briefSummary":73,"conditions":74,"keywords":76,"overallStatus":36,"whyStopped":10,"lastUpdateSubmitDate":80,"lastUpdatePostDateStruct":81,"startDateStruct":84,"completionDateStruct":86,"leadSponsor":88,"locationsCount":89},{"fullName":5,"class":6},"Ann & Robert H Lurie Children's Hospital of Chicago","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"ICU Population",null,"Patients admitted to one of 3 ICUs at Lurie Childrens",[13],"Device: Wireless Wearable Vital Sign Monitor",{"label":15,"type":10,"description":16,"interventionNames":17},"Non-ICU Population","Healthy volunteers who are under 18 years of age, whose parents consent to their participation, and who are willing to visit CAMP for a one time study visit can participate in this study.",[13],[19],{"type":20,"name":21,"description":22,"armGroupLabels":23,"otherNames":10},"DEVICE","Wireless Wearable Vital Sign Monitor","Placement of wireless wearable vital sign monitors on patients limbs for up to 48 hours",[9,15],[25,30],{"name":26,"role":27,"phone":28,"phoneExt":10,"email":29},"Susan Slattery, MD","CONTACT","312-227-3300","sslattery@luriechildrens.org",{"name":31,"role":27,"phone":28,"phoneExt":10,"email":32},"Casey Rand, MDS","crand@luriechildrens.org",[34,49],{"facility":35,"status":36,"city":37,"state":38,"zip":39,"country":40,"cosmosGeoPoint":41,"geoPoint":46,"contacts":47},"Ann & Robert H. Lurie Children's Hospital of Chicago","RECRUITING","Chicago","Illinois","60611","United States",{"type":42,"coordinates":43},"Point",[44,45],-87.65005,41.85003,{"lat":45,"lon":44},[48],{"name":26,"role":27,"phone":28,"phoneExt":10,"email":29},{"facility":50,"status":36,"city":37,"state":38,"zip":39,"country":40,"cosmosGeoPoint":51,"geoPoint":53,"contacts":54},"Northwestern Medicine Prentice Women's Hospital",{"type":42,"coordinates":52},[44,45],{"lat":45,"lon":44},[55],{"name":26,"role":27,"phone":28,"phoneExt":10,"email":29},{"type":57,"investigatorFullName":58,"investigatorTitle":59,"investigatorAffiliation":5,"oldNameTitle":10,"oldOrganization":10},"PRINCIPAL_INVESTIGATOR","Susan Slattery","Attending Physician","100418049",false,"NCT04723654","Evaluating Wearable Smart Sensors for Continuous Measurement of Vital Signs in ICU Patients","Evaluating Wearable Smart Sensors for Continuous Measurement of Vital Signs in ICU","Inclusion Criteria-ICU Population:\n\n* Admitted to one of the four ICUs at Lurie Children's or Prentice Women's Hospital\n* Under 18 years of age\n\nInclusion Criteria-Non-ICU Population\n\n* Under 18 years of age\n* Willing to visit the Center for Autonomic Medicine in Pediatrics (CAMP) for a one time study visit\n\nExclusion Criteria-ICU Population:\n\n* A skin abnormality that would potentially increase the risk of device\n* 18 years of age or older\n* Determined by an attending physician or bedside care team to be too unstable (patient) or experiencing too much stress (family)\n\nExclusion Criteria-Non-ICU Population:\n\n* A skin abnormality that would potentially increase risk of device use\n* 18 years of age or older",true,"ALL","18 Years",{"count":70,"type":71},500,"ESTIMATED","OBSERVATIONAL","The purpose of this study is to develop biocompatible wireless electronic devices that will allow continuous, non-invasive hemodynamic and physiology measurements in the ICU.",[75],"Prematurity",[77,78,79],"Blood Pressure","Vital Signs","Wireless Monitoring","2024-11-25",{"date":82,"type":83},"2024-11-27","ACTUAL",{"date":85,"type":83},"2018-03-15",{"date":87,"type":71},"2026-06-30",{"name":5,"class":6},2]