Status:
COMPLETED
Propofol Versus Alfentanil Versus Nitrous Oxide for Moderate Procedural Sedation
Lead Sponsor:
Hennepin Healthcare Research Institute
Conditions:
Sedation
Eligibility:
All Genders
18+ years
Phase:
PHASE4
Brief 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
Eligibility Criteria
Inclusion
- Adults undergoing moderate procedural sedation in the Emergency Department
Exclusion
- Age \<18 years
- Pregnancy
- Intoxication
- Cannot give informed consent
- Allergy to any of the three study medications
- ASA physical status score \> 2
- Patients who require deep procedural sedation
Key Trial Info
Start Date :
October 1 2009
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
April 1 2015
Estimated Enrollment :
126 Patients enrolled
Trial Details
Trial ID
NCT00997126
Start Date
October 1 2009
End Date
April 1 2015
Last Update
January 27 2017
Active Locations (1)
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1
Hennepin County Medical Center
Minneapolis, Minnesota, United States, 55415