[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100418049":3},{"organization":4,"armGroups":7,"interventions":18,"overallOfficials":10,"centralContacts":24,"locations":33,"responsibleParty":57,"collaborators":10,"id":61,"slug":10,"hasResults":62,"nctId":63,"briefTitle":64,"officialTitle":65,"acronym":10,"eligibilityCriteria":66,"healthyVolunteers":67,"sex":68,"minAge":10,"maxAge":69,"enrollmentInfo":70,"targetDuration":10,"studyType":73,"phases":10,"briefSummary":74,"conditions":75,"keywords":77,"overallStatus":36,"whyStopped":10,"lastUpdateSubmitDate":81,"lastUpdatePostDateStruct":82,"startDateStruct":85,"completionDateStruct":87,"leadSponsor":89,"locationsCount":90},{"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",[34,50],{"facility":35,"status":36,"city":37,"state":38,"zip":39,"country":40,"countryCode":41,"cosmosGeoPoint":42,"geoPoint":47,"contacts":48},"Ann & Robert H. Lurie Children's Hospital of Chicago","RECRUITING","Chicago","Illinois","60611","United States","US",{"type":43,"coordinates":44},"Point",[45,46],-87.65005,41.85003,{"lat":46,"lon":45},[49],{"name":26,"role":27,"phone":28,"phoneExt":10,"email":29},{"facility":51,"status":36,"city":37,"state":38,"zip":39,"country":40,"countryCode":41,"cosmosGeoPoint":52,"geoPoint":54,"contacts":55},"Northwestern Medicine Prentice Women's Hospital",{"type":43,"coordinates":53},[45,46],{"lat":46,"lon":45},[56],{"name":26,"role":27,"phone":28,"phoneExt":10,"email":29},{"type":58,"investigatorFullName":59,"investigatorTitle":60,"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":71,"type":72},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.",[76],"Prematurity",[78,79,80],"Blood Pressure","Vital Signs","Wireless Monitoring","2024-11-25",{"date":83,"type":84},"2024-11-27","ACTUAL",{"date":86,"type":84},"2018-03-15",{"date":88,"type":72},"2026-06-30",{"name":5,"class":6},2]