Patient controlled sedation with propofol for emergency department procedures

Phase 4

Recruiting

• Conditions: Procedural sedation in the emergency department; Anaesthesiology - Pain management; Anaesthesiology - Anaesthetics

• Registration Number: ACTRN12607000548437
• Lead Sponsor: Royal Brisbane and Women's Hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2007-10-24
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 160

Inclusion Criteria

Patient requiring a procedural sedation as part of their treatment in the emergency department

Exclusion Criteria

Inadequate English language comprehension,
Physical inability to use the handset of a patient-controlled infusion pump,
Known allergy or hypersensitivity to propofol,
Anticipated airway difficulty,
Pregnancy

Pregnancy.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Total propofol dose[At end of procedural sedation]

Secondary Outcome Measures

Name	Time	Method
ength of sedation, depth of sedation, patient satisfaction, ease of procedure for the clinician and adverse event rates[At end of procedural sedation]