[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100649210":3},{"organization":4,"armGroups":7,"interventions":13,"overallOfficials":20,"centralContacts":25,"locations":32,"responsibleParty":50,"collaborators":19,"id":53,"slug":54,"hasResults":55,"nctId":56,"briefTitle":57,"officialTitle":58,"acronym":19,"eligibilityCriteria":59,"healthyVolunteers":55,"sex":60,"minAge":19,"maxAge":19,"enrollmentInfo":61,"targetDuration":19,"studyType":64,"phases":65,"briefSummary":67,"conditions":68,"keywords":73,"overallStatus":35,"whyStopped":19,"lastUpdateSubmitDate":79,"lastUpdatePostDateStruct":80,"startDateStruct":83,"completionDateStruct":85,"leadSponsor":87,"locationsCount":88},{"fullName":5,"class":6},"McGill University Health Centre\u002FResearch Institute of the McGill University Health Centre","OTHER",[8],{"label":9,"type":6,"description":10,"interventionNames":11},"Wireless Near-infrared spectroscopy (NIRS)","Wireless NIRS applied to participant's forehead.",[12],"Device: Wireless NIRS",[14],{"type":15,"name":16,"description":17,"armGroupLabels":18,"otherNames":19},"DEVICE","Wireless NIRS","Wireless NIRS applied to participant forehead.",[9],null,[21],{"name":22,"affiliation":23,"role":24},"Guilherme Sant'Anna, MD, PhD","RI-MUHC","PRINCIPAL_INVESTIGATOR",[26],{"name":27,"role":28,"phone":29,"phoneExt":30,"email":31},"Alyssa Maximov, BSc","CONTACT","5149341934","78229","alyssa.maximov@muhc.mcgill.ca",[33],{"facility":34,"status":35,"city":36,"state":37,"zip":38,"country":39,"countryCode":40,"cosmosGeoPoint":41,"geoPoint":46,"contacts":47},"Montreal Children's Hospital","RECRUITING","Montreal","Quebec","H3H2R9","Canada","CA",{"type":42,"coordinates":43},"Point",[44,45],-73.58781,45.50884,{"lat":45,"lon":44},[48],{"name":22,"role":28,"phone":29,"phoneExt":30,"email":49},"guilherme.santanna@mcgill.ca",{"type":24,"investigatorFullName":51,"investigatorTitle":52,"investigatorAffiliation":5,"oldNameTitle":19,"oldOrganization":19},"Guilherme Sant'Anna, MD","Neonatologist","100649210","evaluating-a-wireless-nirs-device-in-the-neonatal-intensive-care-unit-100649210",false,"NCT07732244","Evaluating a Wireless NIRS Device in the Neonatal Intensive Care Unit","Evaluating a Wireless NIRS Device in the Neonatal Intensive Care Unit: a Sub-study of the Wireless NICU Study","Inclusion Criteria:\n\n* Infants admitted to the NICU with a gestational age of ≥ 32 weeks at the time of the monitoring\n* undergoing monitoring with the INVOS wired NIRS system.\n\nExclusion Criteria:\n\n* Infants with a skin abnormality that would potentially increase the risk of injury,\n* Patient too unstable or family experiencing too much stress as determined by an attending physician or bedside care team to not be approached for recruitment.","ALL",{"count":62,"type":63},20,"ESTIMATED","INTERVENTIONAL",[66],"NA","The wireless NIRS sensor will be placed on the participant's forehead, directly underneath the INVOS wired sensor. The wireless NIRS sensor will remain in place for 4 consecutive hours, over 2 consecutive days. As standard-of-care, nursing personnel removes all sensors at every care to evaluate skin and reduce the risk of pressure sores. The wireless NIRS device will be removed and reapplied at the same time, by the research team who will annotate what time the sensor was removed, replaced, and the condition of the skin. This will be used to correlate signal disconnection with sensor care (i.e., skin checks, sensor removal, etc.).",[69,70,71,72],"Hypoxic-Ischemic Encephalopathy","Congenital Heart Disease","Stroke Hemorrhagic","Aneurysm Cerebral",[74,75,76,77,78],"NIRS","Near-Infrared Spectroscopy","Wireless Sensor","Technology","NICU","2026-07-27",{"date":81,"type":82},"2026-07-28","ACTUAL",{"date":84,"type":82},"2025-11-15",{"date":86,"type":63},"2026-12-01",{"name":5,"class":6},1]