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
| Type | Name | Description |
|---|---|---|
| DRUG | Propofol | Propofol 1 mg/kg IV followed by 0.5 mg/kg prn sedation |
| DRUG | Alfentanil | Alfentanil 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.