Effectivness of a new conductive prewarming system to prevent perioperativ hypothermia in ENT surgery

Not Applicable

• Conditions: T68; R68.0; Hypothermia; Hypothermia, not associated with low environmental temperature

• Registration Number: DRKS00004523
• Lead Sponsor: Zentrum für Anästhesiologie, Rettungs- und Intensivmedizin

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2012-11-02
• Study Completion: 2012-12-22
• Results First Posted: 2013-02-14
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 80

Inclusion Criteria

•BMI 20-30 kg/m2
•ASA I-III
•procedure time 60-180 minutes
•Anesthetics: midazolam, remifentanil, propofol, rocuronium, and sevoflurane

Exclusion Criteria

•adipositas permagna
•ASA IV-V
•hypo- or hyperthyroidism
•fever, infectious disease
•pregnancy
•procedure time < 60 minutes or > 180 minutes
•allergie to midazolam, remifentanil, propofol, rocuronium, or sevoflurane

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Duration, degree and incidence of perioperative hypothermia will be measured with an esophageal and forehead temperature probe every 15 minutes.

Secondary Outcome Measures

Name	Time	Method
incidence of postoperativ hypothermia;<br>PACU length of stay