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Clinical Trials/NCT02031159
NCT02031159
Completed
Not Applicable

Correlation, Accuracy, Precision and Practicability of Zero Heat Flux Method in Comparison With Sublingual and Nasopharyngeal Temperature Measurement

University Hospital Schleswig-Holstein1 site in 1 country120 target enrollmentOctober 2013
ConditionsHypothermia

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Hypothermia
Sponsor
University Hospital Schleswig-Holstein
Enrollment
120
Locations
1
Primary Endpoint
body core temperature (°C)
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

Hypothermia is common in patients undergoing general anesthesia. There have been several negative outcomes reported. Zero heat flux is a non-invasive method for measurement of body core temperature. The aim of this study is to see if this method is comparable in terms of correlation, accuracy, precision and practicability to commonly used sublingual and nasopharyngeal temperature monitoring.

Detailed Description

Hypothermia is common in patients undergoing general anesthesia. There have been several negative outcomes reported such as bleeding, infection rate, cardiac complications, prolonged wound healing and patient discomfort. Zero heat flux is a non-invasive method for measurement of body core temperature. The aim of this study is to see if this method is comparable in terms of correlation, accuracy, precision and practicability to commonly used sublingual and nasopharyngeal temperature monitoring. Measurements are performed with the SpotOn® sensor by Arizant Healthcare, Inc..

Registry
clinicaltrials.gov
Start Date
October 2013
End Date
December 2013
Last Updated
11 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
University Hospital Schleswig-Holstein
Responsible Party
Principal Investigator
Principal Investigator

PD Dr. Jan Hoecker

PD Dr. Jan Höcker

University Hospital Schleswig-Holstein

Eligibility Criteria

Inclusion Criteria

  • elective surgery in gynecology or trauma surgery
  • planned surgery time \> 60 min
  • patients older than 16 years

Exclusion Criteria

  • emergency surgery
  • need for post-surgery ventilation
  • patient's denial to take part in the study

Outcomes

Primary Outcomes

body core temperature (°C)

Time Frame: body core temperature taken at 15 min after induction of anesthesia

Secondary Outcomes

  • body core temperature (°C)(body core temperature taken at 45 min after induction of anesthesia)

Study Sites (1)

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