Feedback on Perioperative Temperature Management and Patient Outcomes: Three-arm Trial to Compare Feedback

Not Applicable

Completed

• Conditions: Hypothermia; Surgical Site Infections

• Registration Number: NCT02414191
• Lead Sponsor: Ottawa Hospital Research Institute

Brief Summary

The investigators aim to assess the impact of benchmarked and ranked feedback on anesthesiologists' perioperative temperature management and subsequent patient outcomes.

Detailed Description

Not available

Study Timeline

• Study Start: 2015-02
• Study First Submitted: 2015-03-19
• Study First Submitted QC: 2015-04-09
• Study First Posted: 2015-04-10
• Primary Completion: 2018-04-06
• Study Completion: 2018-04-06
• Status Verified: 2020-03
• Last Update Submitted: 2020-03-20
• Last Update Posted: 2020-03-24

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 45

Inclusion Criteria

• Staff Anesthesiologists at The Ottawa Hospital

Exclusion Criteria

• none

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Patient peri-operative temperature	Within the 30 minutes immediately before or the 15 minutes immediately after anesthesia end time.

Secondary Outcome Measures

Name	Time	Method
Intraoperative warming device usage perioperative	intraoperative
Patient post-operative surgical site infection (SSI) rate	Within 30 days of surgery

Trial Locations

Locations (1)

The Ottawa Hospital; 🇨🇦 Ottawa, Ontario, Canada