[{"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":42},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"id":9,"slug":4,"hasResults":10,"nctId":11,"briefTitle":12,"officialTitle":12,"acronym":13,"eligibilityCriteria":14,"healthyVolunteers":10,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":17,"targetDuration":4,"studyType":20,"phases":21,"briefSummary":23,"conditions":24,"keywords":27,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":30,"lastUpdatePostDateStruct":31,"startDateStruct":34,"completionDateStruct":36,"leadSponsor":38,"locationsCount":41},"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":18,"type":19},80,"ESTIMATED","INTERVENTIONAL",[22],"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.",[25,26],"Average Length of Stay","Surgery",[28],"Remote monitoring","RECRUITING","2026-06-15",{"date":32,"type":33},"2026-06-17","ACTUAL",{"date":35,"type":33},"2026-06-03",{"date":37,"type":19},"2027-02-01",{"name":39,"class":40},"Rhythm Diagnostic Systems","INDUSTRY",4,""]