[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Mode Sensors AS\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":39},{"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":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":23,"conditions":24,"keywords":4,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":28,"lastUpdatePostDateStruct":29,"startDateStruct":32,"completionDateStruct":34,"leadSponsor":36,"locationsCount":5},"100641162","validation-of-a-wearable-bioimpedance-sensor-for-hydration-monitoring-100641162",false,"NCT07655401","Validation of a Wearable Bioimpedance Sensor for Hydration Monitoring","Validation of a Wearable Bioimpedance Sensor for Non-Invasive Monitoring of Hydration Status","VAMOS","Inclusion Criteria:\n\n* Age ≥ 65 years\n* Planned fluid management due to presumed dehydration\n* Expected duration of hospital stay ≥ 3 days\n\nExclusion Criteria:\n\n* Known allergies or skin sensitivities to electrode hydrogel and\u002For acrylic adhesives\n* Implantable pulse generators such as pacemakers and defibrillators, and\u002For use of other electrical medical equipment for which an interaction effect with the investigational device cannot be ruled out.\n* Scheduled MRI\n* Scheduled diathermy\n* Breached skin at device application areas (upper back, anterior thigh and upper arm)\n* Unconsciousness\n* Critically ill (presence of acute organ dysfunction requiring intensive monitoring and management)\n* Any medical or psychiatric condition, which in the opinion of the investigator precludes participation\n* Incapable of giving informed consent","ALL","65 Years",{"count":20,"type":21},60,"ESTIMATED","OBSERVATIONAL","The purpose of the project is to validate the performance of a wearable bioimpedance sensor (Re:Balans®) for monitoring hydration status. The study includes hospitalized patients aged 65 years or older who are admitted to the hospital with suspected dehydration. Data will be collected continuously throughout the hospital stay using one sensor placed on the back, one on the upper arm, and one on the front of the thigh. Sensor measurements will be compared with multiple reference methods for assessing hydration status, including blood tests, body weight and fluid balance charts. Agreement with these reference measures will form the basis for the performance evaluation.\n\nThe anticipated benefit of the project is the validation of a novel, user-friendly, and non-invasive tool for hydration monitoring, with the aim of improving patient care, preventing complications, and reducing the need for hospital readmissions.",[25,26],"Dehydration","Hypovolemia","NOT_YET_RECRUITING","2026-06-15",{"date":30,"type":31},"2026-06-17","ACTUAL",{"date":33,"type":21},"2026-08",{"date":35,"type":21},"2027-03-31",{"name":37,"class":38},"Mode Sensors AS","INDUSTRY",""]