Clinical Trials Directory

Trials / Completed

CompletedNCT03028688

HIFLO ENDO-High Flow Nasal Cannula in GI Endoscopy

HIFLO ENDO- Use of High Flow Nasal Cannula Oxygenation to Increase Patient Safety During Upper GI Endoscopy

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
262 (actual)
Sponsor
University of Maryland, Baltimore · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

Millions of patients undergo upper GI endoscopy in the United States each year. A large number of these patients have anesthesia to assist with their comfort during the procedure. The majority of patients do not have a protected airway during the procedure, meaning there is no endotracheal tube. Instead the current standard of care is to give supplementary oxygen via nasal cannula. Because patients are deeply sedated or have general anesthesia there is a risk for low oxygen saturation during the procedure, which presents a significant patient safety issue. The purpose of the clinical trial is compare the current anesthesia standard of care against high flow nasal cannula oxygen delivery during anesthesia. The investigator's hypothesis is that high flow nasal cannula oxygen delivery will decrease the frequency with which patients experience hypoxemia during anesthesia for upper GI endoscopy.

Conditions

Interventions

TypeNameDescription
DEVICEHigh flow nasal cannula oxygenParticipants will receive high flow nasal cannula oxygen delivery during anesthesia. Participants will also have transcutaneous PCO2 measurements performed using a cutaneous electrode.

Timeline

Start date
2017-06-21
Primary completion
2019-05-09
Completion
2019-05-09
First posted
2017-01-23
Last updated
2022-07-21

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT03028688. Inclusion in this directory is not an endorsement.