Status:
COMPLETED
Nasopharyngeal Versus Nasal Cannula Oxygen Supplementation in Surgery Patients
Lead Sponsor:
Vanderbilt University
Conditions:
Oxygen Administration During Deep Sedation
Eligibility:
All Genders
16+ years
Phase:
NA
Brief 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 sedatio...
Eligibility Criteria
Inclusion
- Patients greater than 16 years of age
- Patients who present for oral surgery or esophagoduodenography and colonoscopy
- Patients who undergo intravenous sedation
Exclusion
- Patients who require endotracheal intubation
- ASA class 4 or higher
- Existing esophageal disease such as a perforation or varices
Key Trial Info
Start Date :
August 1 2014
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
January 1 2016
Estimated Enrollment :
60 Patients enrolled
Trial Details
Trial ID
NCT02219464
Start Date
August 1 2014
End Date
January 1 2016
Last Update
June 1 2017
Active Locations (1)
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1
Vanderbilt University Medical Center
Nashville, Tennessee, United States, 37232