[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100623471":3},{"organization":4,"armGroups":7,"interventions":8,"overallOfficials":7,"centralContacts":18,"locations":7,"responsibleParty":24,"collaborators":26,"id":30,"slug":31,"hasResults":32,"nctId":33,"briefTitle":34,"officialTitle":35,"acronym":36,"eligibilityCriteria":37,"healthyVolunteers":32,"sex":38,"minAge":39,"maxAge":7,"enrollmentInfo":40,"targetDuration":7,"studyType":43,"phases":7,"briefSummary":44,"conditions":45,"keywords":7,"overallStatus":48,"whyStopped":7,"lastUpdateSubmitDate":49,"lastUpdatePostDateStruct":50,"startDateStruct":53,"completionDateStruct":55,"leadSponsor":57,"locationsCount":7},{"fullName":5,"class":6},"Murata Vios, Inc.","INDUSTRY",null,[9],{"type":10,"name":11,"description":12,"armGroupLabels":7,"otherNames":13},"DEVICE","Moni-Patc Temperature Monitoring Patch System","A non-sterile, non-invasive temperature monitoring system applied to the neck; Bluetooth 5.0 transmission to a receiver; continuous core temperature estimation using dual heat-flux\u002Fthermistor-based algorithm; conforms to ISO 80601-2-56 (25-42 °C).",[14,15,16,17],"MP-P20U Sensor","MP-D20U Receiver","MP-S20U Disposable Strips","MP-E20U Extension Cable",[19],{"name":20,"role":21,"phone":22,"phoneExt":7,"email":23},"Ash Shibata Senior Manager","CONTACT","612-497-7397","a.shibata@murata.com",{"type":25,"investigatorFullName":7,"investigatorTitle":7,"investigatorAffiliation":7,"oldNameTitle":7,"oldOrganization":7},"SPONSOR",[27],{"name":28,"class":29},"University of Minnesota","OTHER","100623471","clinical-accuracy-validation-of-the-moni-patc-temperature-monitoring-patch-during-surgery-compared-with-esophageal-and-bladder-temperature-100623471",false,"NCT07397065","Clinical Accuracy Validation of the Moni-Patc Temperature Monitoring Patch During Surgery (Compared With Esophageal and Bladder Temperature)","Moni-Patc Temperature Monitoring Patch System Clinical Accuracy Validation","Moni-Patch OR","Inclusion Criteria:\n\n1. Age ≥18 years\n2. Subject is undergoing an elective surgical procedure expected to require at least 60min of general anesthesia and during which routine esophageal (Teso) and bladder (Tbld) temperature monitoring is expected.\n3. Subjects are expected to remain hospitalized at least overnight after surgery.\n4. Subject specifically agrees to temperature Sensor placement on the neck prior to surgery.\n5. Must be able to attach the Sensor away from the operative field (neck) with uninterrupted wireless connection between the Sensor and the Receiver (as close as possible).\n6. Use environment must meet both of the following parameters:\n\n   1. Temperature 15-40⁰ C\u002F59-104⁰ F\n   2. Humidity 30-75% RH (non-condensing)\n7. For non-English speaking subjects, a translator must be present at the time of consent.\n\nExclusion Criteria:\n\n1. Subjects unable to provide their own consent. Consent from family or LOR is not acceptable.\n2. Subjects undergoing surgical procedures who have conditions of the esophagus or bladder that contraindicate placement of these monitoring probes\u002Fsensor.\n3. Subjects whose surgery does not involve the monitoring of esophageal or bladder temperature.\n4. Subjects undergoing surgery that prohibits placement of an esophageal temperature monitoring probe\u002Fsensor (e.g. neck surgery).\n5. Subjects with medical conditions such as inflammation, scratches, redness, rash at the Sensor placement site.\n6. Subjects for whom the sensor cannot be securely adhered to the skin without floating or detaching, or accurately positioned over the carotid artery.\n7. Not for use in MRI or CT facilities.\n8. Use environment does not meet one or more parameters.","ALL","18 Years",{"count":41,"type":42},30,"ESTIMATED","OBSERVATIONAL","Moni-Patc Temperature Monitoring Patch System, a non-invasive, continuous temperature monitoring device designed to estimate core body temperature by applying a Sensor to the neck.This clinical accuracy validation study aims to verify the accuracy and repeatability of the Moni-Patch compared with an FDA-cleared continuous esophageal and bladder temperature monitoring device used as the clinical reference.Main ObjectivesTo verify that the Moni-Patch and the reference device(esophageal and bladder) demonstrate acceptable agreement, as defined by Bland-Altman Analyses (bias within ±0.4°C and limits of agreement between -1.0°C and 1.0°C).To verify the consistency and repeatability of temperature measurements obtained from the Moni-Patch during continuous monitoring.",[46,47],"Temperature Monitoring","Intraoperative","NOT_YET_RECRUITING","2026-02-05",{"date":51,"type":52},"2026-02-09","ACTUAL",{"date":54,"type":42},"2026-02-06",{"date":56,"type":42},"2026-06-30",{"name":5,"class":6}]