[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100583843":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":19,"centralContacts":20,"locations":19,"responsibleParty":26,"collaborators":19,"id":30,"slug":31,"hasResults":32,"nctId":33,"briefTitle":34,"officialTitle":35,"acronym":36,"eligibilityCriteria":37,"healthyVolunteers":32,"sex":38,"minAge":39,"maxAge":40,"enrollmentInfo":41,"targetDuration":19,"studyType":44,"phases":45,"briefSummary":47,"conditions":48,"keywords":50,"overallStatus":53,"whyStopped":19,"lastUpdateSubmitDate":54,"lastUpdatePostDateStruct":55,"startDateStruct":58,"completionDateStruct":60,"leadSponsor":62,"locationsCount":19},{"fullName":5,"class":6},"Jessa Hospital","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"Remote clinical monitoring","EXPERIMENTAL","The application of remote clinical monitoring after a distal robotic pancreatectomy",[13],"Procedure: Remote clinical monitoring",[15],{"type":16,"name":9,"description":17,"armGroupLabels":18,"otherNames":19},"PROCEDURE","Patients after a distal pancreatectomy will be discharged faster from the hospital and will be remote monitored",[9],null,[21],{"name":22,"role":23,"phone":24,"phoneExt":19,"email":25},"Bjorn Stessel, MD, PhD","CONTACT","+3211222107","bjorn.stessel@jessazh.be",{"type":27,"investigatorFullName":28,"investigatorTitle":29,"investigatorAffiliation":5,"oldNameTitle":19,"oldOrganization":19},"PRINCIPAL_INVESTIGATOR","Stessel Björn","Professor, Dr","100583843","remote-clinical-monitoring-after-robotic-distal-pancreatectomy-100583843",false,"NCT06881602","Remote Clinical Monitoring After Robotic Distal Pancreatectomy","Remote Clinical Monitoring After Robotic Distal Pancreatectomy: a Pilot and Feasibility Study","TOTEM","Inclusion Criteria:\n\n* 18-75 years old\n* Competent to provide informed consent\n* Fluent in Dutch\n* Cognitively capable of understanding and engaging with the study\n* Undergoing robotic distal pancreatectomy\n* Owing a smartphone or has a caregiver who can assist\n* Does not live alone\n* Have a valid national identification number\n\nExclusion Criteria:\n\n* Extended left pancreatectomy\n* Spleen-preserving procedure\n* Residing in a nursing home\n* Patients who are deemed unsuitable for the study by the physician based on clinical evaluation\n* Absence of informed consent or request to not participate in the study","ALL","18 Years","75 Years",{"count":42,"type":43},20,"ESTIMATED","INTERVENTIONAL",[46],"NA","This feasibility trial has three main objectives:\n\n* To investigate the impact of the transmural care pathway TOTeM on the Length of Stay (LOS) for patients undergoing robotic distal pancreatectomy.\n* To investigate the feasibility of the implementation of TOTeM for patients undergoing robotic distal pancreatic surgery, we will measure the recruitment rate by tracking the number of eligible patients who are approached for participation, the percentage who consent to join the study over a specified time period, and the adherence rate which describes how well participants follow the study protocol including the prescribed interventions or follow-up assessments.\n* Assessment of the potential changes in medical costs and outcomes for the purpose of performing a cost-effectiveness analysis from a hospital and patient perspective.",[49],"Digital Health",[51,52],"Remote monitoring","Pancreatectomy","NOT_YET_RECRUITING","2025-09-26",{"date":56,"type":57},"2025-09-29","ACTUAL",{"date":59,"type":43},"2025-10-01",{"date":61,"type":43},"2027-12-31",{"name":5,"class":6}]