ProSed Australasia: A database of procedural sedation practices and outcomes in Australasian Emergency Departments

Not Applicable

Recruiting

• Conditions: Procedural Sedation; Emergency medicine - Other emergency care; Anaesthesiology - Other anaesthesiology

• Registration Number: ACTRN12622000095763
• Lead Sponsor: orthern Sydney Local Health District

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2022-01-24
• Last Update Posted: 16 January 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 10000

Inclusion Criteria

All patients undergoing procedural sedation at a participating site.

Exclusion Criteria

None

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Rate of adverse events experienced by patients undergoing procedural sedation, subclassified into minor/moderate/severe adverse events. These events will be identified by our audit of study records from the form completed by the clinician performing the sedation.[Data will be analysed 6-monthly for 20 years.]

Secondary Outcome Measures

Name	Time	Method
Incidence of hypotension (SBP <90 mmHg) experienced by patients undergoing procedural sedation, stratified by drug used and dose per kilogram. These events will be identified by our audit of study records from the form completed by the clinician performing the sedation.[Data will be analysed annually for 20 years.]