[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"physiological-parameters\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:physiological-parameters":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,48],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":28,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":47},"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":20,"type":21},102,"ESTIMATED","INTERVENTIONAL",[24],"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.",[27],"Physiological Parameters",[29,30,31,32,33,34],"biosensor","early warning score","real care conditions","traumatology","anesthesia","intensive care","NOT_YET_RECRUITING","2026-06-15",{"date":38,"type":39},"2026-06-16","ACTUAL",{"date":41,"type":21},"2026-06",{"date":43,"type":21},"2026-12",{"name":45,"class":46},"Centre Hospitalier Intercommunal de Toulon La Seyne sur Mer","OTHER",1,{"id":49,"slug":50,"hasResults":11,"nctId":51,"briefTitle":52,"officialTitle":53,"acronym":54,"eligibilityCriteria":55,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":56,"enrollmentInfo":57,"targetDuration":4,"studyType":59,"phases":4,"briefSummary":60,"conditions":61,"keywords":64,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":67,"lastUpdatePostDateStruct":68,"startDateStruct":70,"completionDateStruct":72,"leadSponsor":74,"locationsCount":4},"100625558","physiological-benefits-from-the-removal-of-tracheostomy-tubes-obtained-via-wearable-devices-100625558","NCT07424196","Physiological Benefits From the Removal of Tracheostomy Tubes (Obtained Via Wearable Devices)","Collect Physiological Data of Patients Before and After Tracheostomy Tube Removal Using Wearable Devices to Quantify Physiological Benefits of Decannulation","RVTR1","Inclusion Criteria:\n\n* 18 years≤Age≤90 years, non-mechanically ventilated patients.\n* Tracheotomy completed, ≥48 hours since cannula placement (postoperative early edema has stabilized).\n* Patient or legal representative has provided informed consent.\n* Following our department's 2018 decannulation procedure, patients who successfully completed decannulation\n\nExclusion Criteria:\n\n* Patients with abnormal skin conditions preventing continuous wearing of monitoring devices;\n* Interruption of physiological monitoring data;\n* Poor quality of physiological monitoring data;\n* Recent (≤48 hours) major neck\u002Fupper airway surgery requiring avoidance of upper airway airflow impact.\n* Severe consciousness disorder\u002Fdelirium (RASS ≤ -3 or ≥ +2), extreme anxiety\u002Finability to cooperate.\n* Total laryngectomy or laryngo-tracheal separation.\n* Age \\\u003C18 years, Age \\> 90years.\n* Malignant tumor with an expected survival time ≤ 6 months.\n* Patients or legal representatives unable to obtain informed consent.\n* Known contraindications for tracheotomy decannulation.\n* Unable to comply with the use of wearable devices","90 Years",{"count":58,"type":21},60,"OBSERVATIONAL","The population included in this study consists of tracheostomy patients admitted to the pulmonary department of Beijing Rehabilitation Hospital, undergoing decannulation rehabilitation treatment. After the patient is admitted, the research team evaluates whether they are suitable to enter the decannulation process. For enrolled patients, a 24-hour wearable device is worn upon admission to record physiological parameters.\n\nPatients, following clinical and rehabilitation treatment, can start using a \"speaking valve\" as soon as their condition permits. Within the first 24 hours prior to the initial use of the speaking valve, wearable devices may be utilized a second time to gather data.\n\nPatients successfully completed the decannulation process, tolerating the speaking valve for 4 hours (PEF\u002FPCF ≥ 100liters\u002Fmin).The wearable device was utilized to gather 24 hours physiological parameters for the third time within the 24 hours leading up to decannulation.\n\nPatients who underwent successful decannulation had physiological parameters collected for the forth time using wearable devices within 24 hours prior to discharge.\n\nThis study preliminarily compares the differences in physiological parameters at four time points (within 24 hours of admission, within 24 hours prior to using a speaking valve, within 24 hours prior to decannulation and within 24 hours before discharge), predicts the physiological benefits of decannulation for patients, and advocates for the concept of \"early decannulation.\" Decannulation criteria: If the patient can tolerate wearing the speaking valve continuously for 4 hours (gradually increasing the duration: 30 minutes, 1 hour, 2 hours, 4 hours), and if PEF\u002FPCF ≥ 100 liters\u002Fmin, planned removal of the tracheostomy tube can be considered.\n\nCriteria for successful decannulation: Patients who successfully completed the decannulation process and had their tubes removed, with no reinsertion of the tracheostomy tube or endotracheal intubation within 48 hours after decannulation.",[27,62,63],"Wearable Devices","Tracheostomy Decannulation",[65,27,62,66],"speaking valve","Tracheostomy decannulation","2026-05-30",{"date":69,"type":39},"2026-06-03",{"date":71,"type":21},"2026-06-01",{"date":73,"type":21},"2027-03-30",{"name":75,"class":46},"Bin Zhang"]