NCT06704867
High Flow Nasal Cannula Compared to Standard Oxygen for Endoscopic Ultrasound
Enrolling by Invitation
NAAges 18+InterventionalSupportive careMayo ClinicInvestigator-initiated
~200 participants
Updated 2026-01-07 on ClinicalTrials.gov
What's tested:High flow nasal cannula
At a glance
Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Decrease recovery time
Measured over 4 hours
Conditions
Where it's being run
1 sites across 1 statesMinnesota1
Study leadership
- Bhargavi Gali, MD, MHA · PRINCIPAL_INVESTIGATOR · Mayo Clinic
Who to contact
This trial hasn't published a contact. View it on ClinicalTrials.gov
Do you actually qualify for this trial?
Add a private profile and we'll compare every criterion below against your situation — and tell you which ones are met, uncertain, or excluding.
Eligibility criteria
Exclusion
Need for general anesthesia for the procedure instead of the standard monitored anesthesia care.
Patients undergoing combined procedure: Therapeutic EUS/combined procedures including EUS/ERCP, EUS/colonoscopy
Patients on home oxygen therapy, or the diagnosis of "severe COPD"
Patients with existing tracheostomy
Inpatients undergoing EUS
Inability to consent
Cognitive impairment
Blocked nasal passages
Trauma/previous surgery to the nasopharynx
Irregularities of the nose, face, or airway such that HFNC cannot be properly fitted
What this trial measures
- Decrease recovery time4 hours
Time measured in minutes for participants to enter post anesthesia care until the nurse marks "ready for discharge" in the medical record.