Vanderbilt University Medical Center
Nashville, Tennessee, 37232, United States
NCT Number: NCT02219464
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.
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Notify Me16 year and older
All sexes
Interventional
Not applicable
Nashville, Tennessee, 37232, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Initially set at 3 liters/minute
Midazolam 2mg IV, Fentanyl 100mcg IV, Propofol 100 mcg/kg/min. Additional doses of propofol at the discretion of the attending anesthesiologist.
Time frame: During surgical procedure
Time frame: During surgical procedure
(jaw lift, tongue retraction, oral airway placement, mask ventilation, increase in oxygen flow rate, ect.).
Vanderbilt University
Other
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