Evaluation of a Licensed Double-sensor-heat-flux (DHF) Non-invasive Core Temperature Sensor in Small Children and Toddlers Undergoing Surgery

Hypothermia; Anesthesia Clinical Trial

Official title:

Evaluation of a Licensed Double-sensor-heat-flux (DHF) Non-invasive Core Temperature Sensor in Small Children and Toddlers Undergoing Surgery

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05516771
• Other study ID #: DHF-TaSC
• Status: Completed
• Start date: October 1, 2022
• Est. completion date: February 26, 2023

Study information

• Verified date: March 2023
• Source: Medical University of Vienna
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

Title: Evaluation of a licensed double-sensor-heat-flux (DHF) non-invasive core temperature sensor in small children and toddlers undergoing surgery.

CI/PS identification code: DHF-TaSC Device Name: Tcore™ system (Tcore-Adapter MP00999 & Tcore-Sensor MP 00989) Manufacturer: Drägerwerk AG & CO KGaA Study design: Prospective, single arm, clinical study

Patients:

• Number: 72

• Age / gender: females and males between 0 and 7 years

• Patients of a tertiary referral, university-affiliated hospital undergoing surgery

Exclusion Criterions:

• Operation site, rash or infection that prevents the application of the heat flux thermometers.

• Patients and/or legal guardians not willing to participate in the trial.

• Patients older than 7 years Setting: ORs of a tertiary referral, university-affiliated hospital. Study variables: measurement triplets measured via two double-sensor-heat-flux (DHF) thermometer the Tcore™ (Dräger, Drägerwerk AG & Co KG, 23558 Lübeck, Germany) one placed on the forehead and one on the upper belly and temperature measured by a rectally placed temperature probe.

Description:

Body temperature is important for maintaining normal physiological functions. Inadvertent hypothermia as well as pyrexia are associated with higher morbidity and mortality. Consequently, continuous measurement of body temperature is standard of care at intensive care units (ICUs) and in operation rooms (ORs). The use of core temperature measurements such as pulmonary catheter (gold standard), esophageal or urinary probes is recommended because of higher accuracy than non-invasive measuring methods. The double-sensor-heat-flux (DHF) thermometer the Tcore™ (Dräger, Drägerwerk AG & Co KG, 23558 Lübeck, Germany). The DHF thermometers consist of two sensors separated by a known thermal resistance. One side is placed directly at the patient's skin and the other is facing the environment. After some equilibration time the core temperature can then be calculated. To date no study, exist for the use of the Tcore™ thermometer in children or toddlers. Children are at higher risk for hypothermia and perioperative hypothermia is still common in children.(8) The objective is to find a non-invasive core temperature measurement for children to guide perioperative temperature management.

Primary Objective (Hypothesis):

Evaluation of the accuracy of the licensed double-sensor-heat-flux (DHF) thermometer the Tcore™ (Dräger, Drägerwerk AG & Co KG, 23558 Lübeck, Germany) when used for intraoperative core temperature measurement in small children and toddlers.

The Hypothesis is that each of the two temperature measurements obtained with the Tcore™ (forehead, upper belly) have a high level of agreement(<0.5°C) with the standard of care temperature measurements via rectal temperature probe.

Our primary objective is to investigate the agreement between the two temperature measurements obtained with the Tcore™ (Dräger, Drägerwerk AG & Co KGaA, 23558 Lübeck, Germany) placed on the forehead and the upper belly and temperature measured via a rectally placed Medical Level 1 disposable General Purpose Temperature Probe (Smiths Medical Österreich GmbH, Brunn am Gebirge, Austria). Measure triplets of the two Tcore™ sensors and the rectally placed probe are obtained every 3 minutes for up to 12 consecutive hours or for the duration the patient spends in the OR and the recovery room. If the observed limits of agreement (± 1.96 SD around the mean difference), within which 95% of the differences are expected to fall, are clinically acceptable, the methods are considered to agree. We define deviations of +/-0.5°C, a priori, to be acceptable for the Bland Altman method comparison analysis as was done in previous studies.

Intended use The Tcore system is a thermometer intended for non-invasive, continuous measurement of the core body temperature of children from 5 years of age, adolescents, and adults. The Tcore system consists of a sensor and an adapter. The adapter is reusable. The sensor is intended for single use. The Tcore system works in adjusted mode, i.e., the core body temperature is determined by a dual sensor.

Off-Label/Investigational Use In context of this clinical study the Tcore-system will be investigated outside its approved and intended use, namely in children below the age of five and toddlers.

Descriptive statistics:

• For nominal and ordinal data absolute frequencies and percentages, fraction, rate, and incidence will be calculated, if appropriate.

• Continuous data are described by mean ± standard deviation (SD) in case of approximate normal distribution, or by median, interquartile range otherwise.

Endpoint analysis:

For the primary objective, a scatterplot of differences between Tcore and standard measurements and their mean will be produced for each of the two Tcore measurements in relation to the measurement standard (rectal temperature). If the differences prove to be approximately independent for the observed range of temperatures, limits of agreement will be calculated using the method by Zou (2013).(23) If these limits are contained within the acceptable deviation of +/-0.5°C the respective Tcore measurement method will be considered acceptable. Irrespective of the success of the investigation of agreement the results for both Tcore measurement locations will be reported.

For the secondary objective sensitivity and specificity will be calculated with 95% confidence intervals for each Tcore measurement in relation to the measurement standard.

All study data will be queried from the ICCA and from the database of electronic health records the Vienna General Hospital information management system (AKIM; "Allgemeines Krankenhaus Informationsmanagement") (Siemens AG Österreich, Vienna, Austria). Intellispace Critical Care and Anesthesia. After acquisition, patient data will be anonymized, cleaned, and stored in a study database.

Patient identification will contain name, sex, and birthdate. This data will be documented in an excel sheet, protected with a password. All patients will be given a number for pseudonymization. The verification key will be stored on a separate computer in our laboratory. Only specially authorized persons (Dr. Sebastian Zeiner and Prof. Oliver Kimberger) will have access to the data.

All data will be stored on a password secured computer in the laboratory of our department (Department for Anesthesia) at the Medical University of Vienna.

At any time, medical confidentiality will be fulfilled by all persons involved in this project.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 58
• Est. completion date: February 26, 2023
• Est. primary completion date: February 26, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 0 Years to 7 Years

Eligibility

Inclusion Criteria:

• 0-7 years

• elective surgical procedures with a procedure time of more than 30 min

• operations for which insertion of a rectal temperature probe is clinically indicated as a routine method, (e.g., operations in regional anaesthesia)

Exclusion Criteria:

• rash or infection that prevents the application of the Heat flux thermometers.

• Fragile forehead skin state;

• known allergy to the probe adhesive or any constituent components

• maxillofacial trauma or lesions

• procedures impeding proper placement of the Tcore™ sensor

• neurologically impaired children with abnormal thermoregulation;

• hemodynamic instability; need for vasoactive medication;

• procedures associated with extended use of abdomino/thoracic rinsing fluids;

• thoracoscopic/thoracotomy procedures;

• malignant hyperthermia or family history of malignant hyperthermia

• patient with fever or infection;

• all conditions that might be judged to abnormally alter skin perfusion

• patients or their legal guardian are not willing to participate in the trial.

Related Conditions & MeSH terms

• Hypothermia
• Hypothermia; Anesthesia

Intervention

Device:
• Tcore™ system
The Tcore sensor is a double-sensor-heat-flux (DHF) thermometer and consist of two sensors separated by a known thermal resistance. One side is placed directly at the patient's skin and the other is facing the environment. After some equilibration time the core temperature can then be calculated. The sensors are placed above the eye and the sinus frontalis. Intended use The Tcore system is a thermometer intended for non-invasive, continuous measurement of the core body temperature of children from 5 years of age, adolescents, and adults. The Tcore system consists of a sensor and an adapter. The adapter is reusable. The sensor is intended for single use. The Tcore system works in adjusted mode, i.e., the core body temperature is determined by a dual sensor. Off-Label/Investigational Use In context of this clinical study the Tcore-system will be investigated outside its approved and intended use, namely in children below the age of five and toddlers.

Locations

Country	Name	City	State
Austria	Medical Univercity Vienna	Vienna

Sponsors (1)

Lead Sponsor	Collaborator
Oliver Kimberger

Country where clinical trial is conducted

Austria, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Accuracy of Tcore core temperature measurements	A scatterplot of differences between Tcore and standard measurements of body temperature,limits of agreement will be calculated using the method by Zou (2013).(23)	For the duration of Anesthesia and a maximum of 12 hours
Secondary	sensitivity and specificity	For the secondary objective sensitivity and specificity will be calculated with 95% confidence intervals for each Tcore measurement in relation to the measurement standard	For the duration of Anesthesia and a maximum of 12 hours