Propofol Versus Alfentanil Versus Nitrous Oxide for Moderate Procedural Sedation
Completed · Phase 4
Conditions studied: Sedation
In brief
This is a clinical trial of propofol and alfentanil as agents for moderated procedural sedation in patients undergoing sedation in the emergency department (ED).
Key facts
- Study ID
- NCT00997126
- Run by
- Hennepin Healthcare Research Institute
- People needed
- 126
- Starts
- 2009-10-01
- Expected to finish
- 2015-04-01
- Last updated by the study team
- 2017-01-27
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Adults undergoing moderate procedural sedation in the Emergency Department
You may not qualify if…
- 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
Where it is running
- Hennepin County Medical Center — Minneapolis, Minnesota, United States
Full record on ClinicalTrials.gov
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