[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"temperature-monitoring\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:temperature-monitoring":26},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,47],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":17,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":27,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":36,"startDateStruct":39,"completionDateStruct":41,"leadSponsor":43,"locationsCount":46},"100631954","non-invasive-temperature-monitoring-in-pediatric-intensive-care-patients-requiring-targeted-temperature-management-evaluation-of-temple-touch-pro-100631954",false,"NCT07507396","Non-invasive Temperature Monitoring in Pediatric Intensive Care Patients Requiring Targeted Temperature Management: Evaluation of Temple Touch Pro","Inclusion Criteria:\n\n1. Age 0 to less than 18 years of age\n2. PICU Diagnosis requiring targeted temperature management. For example traumatic brain injury, cardiac arrest, or anoxic brain injury\n3. Requires continuous temperature monitoring with a foley catheter (bladder) or a general purpose probe placed in the esophagus.\n4. Enrolled within 24 hours of start of continuous temperature monitoring.\n5. Patient has adequate forehead space to accommodate the TTP sensor\n6. Temporal artery perfusion not compromised by injury or other pathology\n7. No surgical procedure planned for 72 hours\n8. Targeted temperature management expected for at least 24 hours at time of consent\n\nExclusion Criteria:\n\n1. Already enrolled in another trial addressing temperature management\n2. Allergy to medical grade acrylic adhesive\n3. Patient does not tolerate placement of TTP sensor on forehead\n4. Contraindication to the placement of two or more of Foley, esophageal, and rectal temperature probes.\n5. A history of skin irritation, skin sensitivity, or skin disease, including psoriasis, eczema, atopic dermatitis, and skin cancer.\n6. Pregnant or lactating female","ALL","0 Years","17 Years",{"count":19,"type":20},20,"ESTIMATED","INTERVENTIONAL",[23],"NA","The purpose of this study is to evaluate the Temple Touch Pro (TTP) in Pediatric Intensive Care Unity (PICU) patients requiring targeted temperature control.",[26],"Temperature Monitoring",[28,29,30,31,32,33],"temperature monitoring","Temple Touch Pro","esophageal","rectum","bladder","temporal artery","NOT_YET_RECRUITING","2026-03-27",{"date":37,"type":38},"2026-04-02","ACTUAL",{"date":40,"type":20},"2026-05",{"date":42,"type":20},"2027-05",{"name":44,"class":45},"Medical College of Wisconsin","OTHER",1,{"id":48,"slug":49,"hasResults":11,"nctId":50,"briefTitle":51,"officialTitle":52,"acronym":53,"eligibilityCriteria":54,"healthyVolunteers":11,"sex":15,"minAge":55,"maxAge":4,"enrollmentInfo":56,"targetDuration":4,"studyType":58,"phases":4,"briefSummary":59,"conditions":60,"keywords":4,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":62,"lastUpdatePostDateStruct":63,"startDateStruct":65,"completionDateStruct":67,"leadSponsor":69,"locationsCount":4},"100623471","clinical-accuracy-validation-of-the-moni-patc-temperature-monitoring-patch-during-surgery-compared-with-esophageal-and-bladder-temperature-100623471","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.","18 Years",{"count":57,"type":20},30,"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.",[26,61],"Intraoperative","2026-02-05",{"date":64,"type":38},"2026-02-09",{"date":66,"type":20},"2026-02-06",{"date":68,"type":20},"2026-06-30",{"name":70,"class":71},"Murata Vios, Inc.","INDUSTRY"]