Trials / Completed
CompletedNCT02219464
Nasopharyngeal Versus Nasal Cannula Oxygen Supplementation in Surgery Patients
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 60 (actual)
- Sponsor
- Vanderbilt University · Academic / Other
- Sex
- All
- Age
- 16 Years
- Healthy volunteers
- Not accepted
Summary
The investigators plan to conduct a randomized, controlled trial comparing nasopharyngeal oxygen supplementation to traditional nasal cannula in patients undergoing oral surgery under moderate sedation.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Nasopharyngeal catheter | |
| DEVICE | Nasal Cannula | |
| PROCEDURE | Oxygen Supplementation | Initially set at 3 liters/minute |
| PROCEDURE | Sedation | Midazolam 2mg IV, Fentanyl 100mcg IV, Propofol 100 mcg/kg/min. Additional doses of propofol at the discretion of the attending anesthesiologist. |
Timeline
- Start date
- 2014-08-01
- Primary completion
- 2015-12-01
- Completion
- 2016-01-01
- First posted
- 2014-08-19
- Last updated
- 2017-06-01
- Results posted
- 2017-06-01
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT02219464. Inclusion in this directory is not an endorsement.