Clinical Accuracy Validation of the Moni-Patc Temperature Monitoring Patch During Surgery (Compared With Esophageal and Bladder Temperature) (Moni-Patch OR)

Murata Vios, Inc.

Status: Not yet enrolling

Conditions: Intraoperative; Temperature Monitoring

Treatments: Device: Moni-Patc Temperature Monitoring Patch System

Study type: Observational

Funder types: Other; Industry

Identifiers

NCT07397065

MM-MPS2-0001

Details and patient eligibility

About

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.

Full description

This single-center, open-label accuracy validation compares continuous core temperature measured by the Moni-Patch applied on the neck with esophageal (T_eso) and bladder (T_bld) temperatures during elective surgeries under general anesthesia. Approximately 30 adult participants will be monitored for ≥60 minutes intraoperatively. Agreement will be assessed using Bland-Altman methods (bias and 95% limits of agreement). The device is non-invasive and Bluetooth-enabled; readings are captured via the receiver and routed to the OR multi-parameter monitor and EMR. Safety monitoring focuses on device-related skin reactions and device deficiencies; no changes to anesthetic care are mandated by the protocol.

Enrollment: 30 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Age ≥18 years

2. 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.

3. Subjects are expected to remain hospitalized at least overnight after surgery.

4. Subject specifically agrees to temperature Sensor placement on the neck prior to surgery.

5. 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).

6. Use environment must meet both of the following parameters:

   1. Temperature 15-40⁰ C/59-104⁰ F
   2. Humidity 30-75% RH (non-condensing)

7. For non-English speaking subjects, a translator must be present at the time of consent.

Exclusion criteria

1. Subjects unable to provide their own consent. Consent from family or LOR is not acceptable.
2. Subjects undergoing surgical procedures who have conditions of the esophagus or bladder that contraindicate placement of these monitoring probes/sensor.
3. Subjects whose surgery does not involve the monitoring of esophageal or bladder temperature.
4. Subjects undergoing surgery that prohibits placement of an esophageal temperature monitoring probe/sensor (e.g. neck surgery).
5. Subjects with medical conditions such as inflammation, scratches, redness, rash at the Sensor placement site.
6. Subjects for whom the sensor cannot be securely adhered to the skin without floating or detaching, or accurately positioned over the carotid artery.
7. Not for use in MRI or CT facilities.
8. Use environment does not meet one or more parameters.