Nasopharyngeal Versus Nasal Cannula Oxygen Supplementation in Surgery Patients
| Status: | Recruiting |
|---|---|
| Healthy: | No |
| Age Range: | 16 - Any |
| Updated: | 4/21/2016 |
| Start Date: | August 2014 |
| End Date: | July 2016 |
| Contact: | Bret Alvis |
| Email: | bret.d.alvis@Vanderbilt.Edu |
| Phone: | 615-343-6268 |
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.
oxygen supplementation to traditional nasal cannula in patients undergoing oral surgery
under moderate sedation.
Inclusion Criteria:
- Patients greater than 16 years of age
- Patients who present for oral surgery or esophagoduodenography and colonoscopy
- Patients who undergo intravenous sedation
Exclusion Criteria:
- Patients who require endotracheal intubation
- ASA class 4 or higher
- Existing esophageal disease such as a perforation or varices
We found this trial at
1
site
1211 Medical Center Dr
Nashville, Tennessee 37232
Nashville, Tennessee 37232
(615) 322-5000
Principal Investigator: Bret Alvis, MD
Phone: 615-343-6268
Vanderbilt Univ Med Ctr Vanderbilt University Medical Center (VUMC) is a comprehensive healthcare facility dedicated...
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