Temperature Measurement in Surgical and Intensive Care Patients - Comparison of Four Measurement Methods
Temp
Temp
Sponsor study identifier
observational
95
1 country
1
Study Start
April 2014
Date type not reportedThis date has not been verified as actual or estimated.
Primary Completion
January 2023
Actual (reported)Study Completion
January 2023
Actual (reported)Comparison of four methods for measuring temperature perioperatively in patients scheduled for laparoscopic surgery and intensive care patients who are hypo-, normo-and hyper terme; Bladder Monitoring, Nasopharyngeal, SpotOn TM, Zero heat flux method and Temporal Scanner. The study is a single-center, observational study carried out by the Central Surgical and Intensive Section at Vestfold Hospital Trust.
Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.
January 2023
Actual (reported)Click on a node to explore related trials.
Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.
February 6, 2014
Actual (reported)April 2014
Date type not reportedThis date has not been verified as actual or estimated.
August 19, 2014
Actual (reported)January 2023
Actual (reported)January 2023
Actual (reported)Temperature difference measured with different measuring methods
The difference in temperature between the temperature measured by the current reference method bladder temperature and the temperature measured with Temporal Scanner, SpotOn and nasopharynx through the entire operational sequence (from first to last measurement) and three individual measurements at 20 minute intervals of intensive care patients.
Timepoints during surgery; Every 20th minute. In intensive patients: 3 measurements during 1 hour (every 20th minute)
Number of patients with 1) Sore after Sticker (SpotOn) 2) epistaxis during hospital stay as a measure of safety and tolerability.
Hospital discharge
Laparoscopic surgery and in ICU patients
Vestfold Hospital Trust
Tønsberg, 3103, Norway
Espen Lindholm, M.D.
Departement of Anesthesiology, Vestfold Hospital Trust
95 participants (actual enrollment reported by the registry).
First Submitted
February 6, 2014
First Posted
August 19, 2014
Study Start
April 2014
Date type not reportedThis date has not been verified as actual or estimated.
Experimental hypothermia using cold ambient temperature and drug-induced inhibition of shivering in awake, healthy volunteers: a crossover, double blinded trial
Study of a New Clinical Device for Reducing Body Core Temperature
Contact the study team to confirm eligibility.
Primary Completion
January 2023
Actual (reported)Study Completion
January 2023
Actual (reported)Last Updated
January 4, 2023
Record last verified: 2023-01
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Source: ClinicalTrials.gov.
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