[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"average-length-of-stay\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:average-length-of-stay":26},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":28,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":32,"startDateStruct":35,"completionDateStruct":37,"leadSponsor":39,"locationsCount":42},"100632484","assessment-of-the-feasibility-and-organisational-impact-of-a-care-pathway-incorporating-the-multisense-medical-device-for-post-operative-home-monitoring-of-elderly-patients-100632484",false,"NCT07514286","Assessment of the Feasibility and Organisational Impact of a Care Pathway Incorporating the MultiSense® Medical Device for Post-operative Home Monitoring of Elderly Patients.","IMPACT - MS","Inclusion Criteria :\n\n* Patient aged 65 or over\n* Patient eligible for remote monitoring using the MultiSense® device\n* No psychiatric illness that would prevent them from giving informed consent or receiving optimal treatment and follow-up care\n* Subject affiliated with a health insurance scheme\n* Subject able to read and understand English\n* Subject who has signed an informed consent form\n* Subjects indicated for scheduled surgery\n* Patients indicated for scheduled surgery :\n\n  * Transverse colectomy, by laparotomy\n  * Hepatic laparoscopy\n  * Laparoscopic or laparoscopic liver surgery (code hlfc or hlfa for procedures)\n  * Hysterectomy\n  * Adnexectomy\n  * Parietal surgery (eventration)\n  * Rectal resection\n  * Right and left colectomy\n  * Stoma closure by direct approach\n\nExclusion Criteria :\n\n* Patients already participating in an interventional clinical trial.\n* Patients subject to legal protection measures, guardianship, curatorship, or deprived of their liberty by judicial or administrative decision.\n* Patients hospitalised without consent.\n* Patients unable to complete a questionnaire and without a close relative to assist them in using the solution.\n* Patients admitted to or residing in a health or social care facility (other than for the surgery itself).\n* Persons admitted to or residing in a health or social care institution (other than for the surgery itself);\n* Persons unable to give their free and informed consent.","ALL","65 Years",{"count":19,"type":20},80,"ESTIMATED","INTERVENTIONAL",[23],"NA","Assessing the clinical and organisational impact of a home-based post-operative monitoring strategy incorporating the MultiSense® device involving 80 patients aged 65 years and over who have undergone major surgery.",[26,27],"Average Length of Stay","Surgery",[29],"Remote monitoring","RECRUITING","2026-06-15",{"date":33,"type":34},"2026-06-17","ACTUAL",{"date":36,"type":34},"2026-06-03",{"date":38,"type":20},"2027-02-01",{"name":40,"class":41},"Rhythm Diagnostic Systems","INDUSTRY",4]