[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100595848":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":19,"centralContacts":19,"locations":20,"responsibleParty":41,"collaborators":19,"id":43,"slug":44,"hasResults":45,"nctId":46,"briefTitle":47,"officialTitle":48,"acronym":49,"eligibilityCriteria":50,"healthyVolunteers":45,"sex":51,"minAge":52,"maxAge":19,"enrollmentInfo":53,"targetDuration":19,"studyType":56,"phases":57,"briefSummary":59,"conditions":60,"keywords":62,"overallStatus":69,"whyStopped":19,"lastUpdateSubmitDate":70,"lastUpdatePostDateStruct":71,"startDateStruct":74,"completionDateStruct":76,"leadSponsor":78,"locationsCount":79},{"fullName":5,"class":6},"Centre Hospitalier Intercommunal de Toulon La Seyne sur Mer","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"Patients managed in anesthesia, rehabilitation\u002Finstensive care unit and traumatology services.","EXPERIMENTAL","Demonstrate the relevance of the data collected from patients treated in different hospital departments, including critical emergencies, intensive care, general intensive care units, and the operating room.",[13],"Other: Continuous monitoring of vital constants with OXYFLEX® biosensor.",[15],{"type":6,"name":16,"description":17,"armGroupLabels":18,"otherNames":19},"Continuous monitoring of vital constants with OXYFLEX® biosensor.","The comparison of physiological data (heart rate, respiratory rate, temperature, pulse oxygen saturation, hemoglobin levels) collected by the OXYFLEX® biosensor with those obtained through standard monitoring over a maximum duration of 10 hours.",[9],null,[21],{"facility":22,"status":19,"city":23,"state":24,"zip":25,"country":26,"countryCode":27,"cosmosGeoPoint":28,"geoPoint":33,"contacts":34},"HIA Ste Anne","Toulon","Var","83000","France","FR",{"type":29,"coordinates":30},"Point",[31,32],5.92836,43.12442,{"lat":32,"lon":31},[35],{"name":36,"role":37,"phone":38,"phoneExt":39,"email":40},"Quentin Mathais, MD","CONTACT","04 83 16 22 05","+33","quentin.mathais@intradef.gouv.fr",{"type":42,"investigatorFullName":19,"investigatorTitle":19,"investigatorAffiliation":19,"oldNameTitle":19,"oldOrganization":19},"SPONSOR","100595848","monitoring-of-patient-physiological-parameters-in-real-life-using-oxyflex-biosensors-versus-standard-monitoring-100595848",false,"NCT07037784","Monitoring of Patient Physiological Parameters in Real Life Using OXYFLEX® Biosensors Versus Standard Monitoring","Monitoring of Physiological Parameters in Real Life in Patients Managed in Anesthesia, Rehabilitation\u002FIntensive Care Unit and Traumatology Services, Using OXYFLEX® Biosensors Versus Standard Monitoring","OXYVIVO","Inclusion Criteria:\n\n* Adult patient (≥ 18 years old);\n* Patient taken care of :\n* in severe traum pathway in the emergency services department\n* or in the operating room for a general anesthesia procedur or locoregional anesthesia planned for a surgical duration grater than 2 hours\n* or admitted to intesive care\u002F general intensive care units.\n\nExclusion Criteria:\n\n* Opposition from the patient or their family to participate in the research ;\n* Pregnant, parturient or breastfeeding woman ;\n* Patient under judical protection (guardianship, curatorship …) or legal safeguarding ;\n* Inability to wear the headband and the sensor (in particular : intracranial neurosurgery, othorhinolaryngology or maxillofacial surgery, debilitating trauma to the head or face …) ;\n* Any other reason that, in the investigator's opinion, could interfere with the evaluation of the study objectives.","ALL","18 Years",{"count":54,"type":55},102,"ESTIMATED","INTERVENTIONAL",[58],"NA","The purpose of this study is to use the OXYFLEX® device in real care conditions during the hospital management of a population of patients from various hospital services. These services include patients from the severe trauma pathway, intensive care, the polyvalent intensive care unit, and the operating room. The objective is to assess the reliability of the data collected by the OXYFLEX® biosensor compared to those obtained from standard monitoring used in these different services and conditions.",[61],"Physiological Parameters",[63,64,65,66,67,68],"biosensor","early warning score","real care conditions","traumatology","anesthesia","intensive care","NOT_YET_RECRUITING","2026-06-15",{"date":72,"type":73},"2026-06-16","ACTUAL",{"date":75,"type":55},"2026-06",{"date":77,"type":55},"2026-12",{"name":5,"class":6},1]