Development and validation of a diagnostic alarm for monitoring anaesthesia related adverse events

Not Applicable

• Conditions: Adverse events during anaesthesia; Anaesthesiology - Other anaesthesiology

• Registration Number: ACTRN12606000319572
• Lead Sponsor: Michael Harrison

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2006-07-24
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: ot yet recruiting
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

Patients having moderate to major surgery where blood loss is expected.

Exclusion Criteria

Inability to give informed consent.

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Detection of adverse events[Throughout the duration of anaesthesia]

Secondary Outcome Measures

Name	Time	Method
Agreement between computer and clinician, throughout the duration of the anaesthetic.[]