Comparison of Oxygenation Between Nasal PAP vs Nasal During Propofol-based Sedation for EUS

Stopped early · Not applicable

Conditions studied: Endoscopic Ultrasound

In brief

Randomized controlled single site study involves oxygenation, continuous positive airway pressure, and ventilation of subject via nasal mask and oxygenationvia closed facemask. The intervention of the study are delivery form of supplemental oxygen, bag-mask ventilation, and continuous nasal CPAP intraoperatively and in the post anesthesia care period.

Key facts

Study ID

NCT04306211

Run by

Indiana University

People needed

11

Starts

2020-12-14

Expected to finish

2022-03-30

Last updated by the study team

2022-11-03

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Age 18 years of age or older
• Patients undergoing upper endoscopic ultrasound
• American Society of Anesthesiology (ASA) Physical Status I-III
• BMI ≥35 kg/m2 or documented Obstructive Sleep Apnea
• Has provided written informed consent

You may not qualify if…

• Inpatient status
• Active Congestive Heart Failure Exacerbation
• Untreated ischemic heart disease
• Acute exacerbation of respiratory disorders, including COPD and asthma
• Emergent procedures
• Pregnancy
• Previous enrollment in this study
• Inability to provide informed consent
• Additional medical testing planned for the same day
• History of allergic reaction to Propofol
• Tracheostomy
• Supra-glottic or sub-glottic tumor
• Gastrointestinal tract obstruction or delayed transit (including delayed gastric emptying, gastric bezoar, achalasia, toxic megacolon).

Where it is running

• Indiana University Health University Hospital — Indianapolis, Indiana, United States
• Indiana University Hospital — Indianapolis, Indiana, United States

Full record on ClinicalTrials.gov

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