Moderate Versus Deep Procedural Sedation With Propofol in the Emergency Department

• Status: Completed
• Trial end date: 2018-12-01
• Target enrollment: 0
• Participant gender: All

Summary

This study is a clinical trial of moderate sedation versus deep sedation with propofol for procedural sedation in the Emergency Department. The purpose of this study is to compare the rate of amnesia and respiratory depression rate in patients who receive moderate sedation to those that receive deep sedation.

• Phase: Phase 4
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Hennepin Healthcare Research Institute; Minneapolis Medical Research Foundation
• Treatments: Hypnotics and Sedatives; Propofol

Criteria

Inclusion Criteria:

• Adults undergoing procedural sedation with propofol in the emergency department

Exclusion Criteria:

• < 18 years old

• Pregnant

• Previous allergic reaction to propofol

• Prisoner

• Unable to provide informed consent