Expired Study
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Nashville, Tennessee 37232


Purpose:

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.


Criteria:

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


NCT ID:

NCT02219464


Primary Contact:

Principal Investigator
Bret Alvis, MD
Vanderbilt University


Backup Contact:

N/A


Location Contact:

Nashville, Tennessee 37232
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: November 18, 2017

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