Peri-operative, unobtrusive core temperature measurement
Recruiting
- Conditions
- nobtrusive core temperature measurement during surgery
- Registration Number
- NL-OMON26681
- Lead Sponsor
- Philips Research
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 40
Inclusion Criteria
≥18 years patients planned to undergo surgery with temperature management as standard part of the procedure. These patients are routinely equipped with an (oesophageal and/or rectal) temperature sensor.
- patients where the expected surgery duration is more than 2 hours.
Exclusion Criteria
- neuro-trauma
- pregnancy
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The comparison of the results from all the sensors
- Secondary Outcome Measures
Name Time Method The observation of the effect of surgery duration and type on the drop in core temperature and observing the comfort and ease of use of the prototype sensors