Clinical Trials Directory

Trials / Completed

CompletedNCT00997126

Propofol Versus Alfentanil Versus Nitrous Oxide for Moderate Procedural Sedation

Propofol Versus Alfentanil Versus Nitrous Oxide for Moderate Procedural Sedation in the Emergency Department

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
126 (actual)
Sponsor
Hennepin Healthcare Research Institute · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This is a clinical trial of propofol and alfentanil as agents for moderated procedural sedation in patients undergoing sedation in the emergency department (ED).

Detailed description

This was initially going to be a trial of propofol vs alfentanil vs nitrous oxide, but our use of nitrous oxide was discontinued before the trial began and the trial was conducted with only two arms

Conditions

Interventions

TypeNameDescription
DRUGPropofolPropofol 1 mg/kg IV followed by 0.5 mg/kg prn sedation
DRUGAlfentanilAlfentanil 10 ug/kg IV followed by 5 ug/kg prn sedation

Timeline

Start date
2009-10-01
Primary completion
2015-04-01
Completion
2015-04-01
First posted
2009-10-19
Last updated
2017-01-27
Results posted
2017-01-27

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00997126. Inclusion in this directory is not an endorsement.