[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Rhythm Diagnostic Systems\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":67},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,43],{"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":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":32,"startDateStruct":35,"completionDateStruct":37,"leadSponsor":39,"locationsCount":42},"100635447","an-evaluation-of-multisense-to-ensure-a-safe-return-home-following-high-risk-gastrointestinal-surgery-compared-with-standard-care-100635447",false,"NCT07552805","An Evaluation of Multisense® to Ensure a Safe Return Home Following High-risk Gastrointestinal Surgery, Compared With Standard Care.","Clinical and Health Economic Evaluation of the Multisense® Solution: Ensuring a Safe Return Home for Patients at High Risk of Complications Following Gastrointestinal Surgery, Compared With the Standard Care Pathway.","SENSE-ECO","Inclusion Criteria :\n\n* Adults (aged 18 and over)\n* Patients scheduled for gastrointestinal surgery :\n* Major gastrointestinal cancer surgery (pancreas, liver, stomach, oesophagus, rectum)\n* Colorectal surgery (rectal resection, surgery on the rectum and anus other than rectal resection, minor or major surgery on the small intestine and colon)\n* Patients in non-critical care with a high risk of post-surgical complications (ASA score 2 or 3)\n* Patients who have a personal mobile phone and Wi-Fi connectivity at home\n* Patients who provide written informed consent to participate in the study\n* Patients who are members of or beneficiaries of a social security scheme\n* Patients who are proficient in French\n\nExclusion Criteria :\n\n* Patients with a contraindication to the use of the device as described in the instructions for use (in particular: known skin allergy to adhesives or silicone, active implantable medical device such as a pacemaker or defibrillator, need for an MRI scan during the intended use of the device, intended application site of the device being tattooed, infected, ulcerated or damaged)\n* Any other condition which, in the investigator's opinion, would compromise the patient's safety or prevent compliance with the requirements of the protocol\n* Pregnant or breastfeeding patient\n* Adult under legal protection (under guardianship, curatorship or judicial protection)\n* Patient already participating in a clinical trial","ALL","18 Years",{"count":20,"type":21},490,"ESTIMATED","INTERVENTIONAL",[24],"NA","The SENSE-ECO study is a prospective, randomized trial of 490 high-risk patients designed to show that the MultiSense® remote monitoring patch safely reduces hospital stays following major digestive surgery. By continuously tracking vital signs for five days at home, the device aims to maintain clinical safety and quality of life while decreasing overall healthcare costs for the French medical system.",[27],"Reduction in the Initial Length of Stay",[29],"Remote monitoring","RECRUITING","2026-06-17",{"date":33,"type":34},"2026-06-22","ACTUAL",{"date":36,"type":21},"2026-06-16",{"date":38,"type":21},"2027-12-19",{"name":40,"class":41},"Rhythm Diagnostic Systems","INDUSTRY",5,{"id":44,"slug":45,"hasResults":11,"nctId":46,"briefTitle":47,"officialTitle":47,"acronym":48,"eligibilityCriteria":49,"healthyVolunteers":11,"sex":17,"minAge":50,"maxAge":4,"enrollmentInfo":51,"targetDuration":4,"studyType":22,"phases":53,"briefSummary":54,"conditions":55,"keywords":58,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":59,"lastUpdatePostDateStruct":60,"startDateStruct":61,"completionDateStruct":63,"leadSponsor":65,"locationsCount":66},"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","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.","65 Years",{"count":52,"type":21},80,[24],"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.",[56,57],"Average Length of Stay","Surgery",[29],"2026-06-15",{"date":31,"type":34},{"date":62,"type":34},"2026-06-03",{"date":64,"type":21},"2027-02-01",{"name":40,"class":41},4,""]