Comparison of a patient warming system using a forced-air, non-compressible under-body mattress versus a regular forced-air underbody mattress system during surgery in pediatrics

Not Applicable

• Conditions: T68; Hypothermia

• Registration Number: DRKS00004200
• Lead Sponsor: Anästhesie, Allgemiene Intensivmedizin und Schmerztherapie

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2012-07-13
• Study Completion: 2013-12-11
• Results First Posted: 2016-01-01
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

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

Inclusion Criteria

children undergoing surgery
- children with a weight under 18kg

Exclusion Criteria

- Patienst under therapeutic hypothermia
- fever

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
80 patients are warmed by 2 different warming systems intraoperatively and measured continous with 4skin electrodes and 1 core temperature electrode.

Secondary Outcome Measures

Name	Time	Method
Differences in skin changes are clinical (visual) evaluated postoperatively