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NOT YET RECRUITING
NCT07591610
NA

Perioperative High-flow Nasal Oxygen in Patients Undergoing Robotic Surgery

Sponsor: Beth Israel Deaconess Medical Center

View on ClinicalTrials.gov

Summary

The aim of the study is to assess whether perioperative use of high-flow nasal oxygen (HFNO) during the period from induction of anesthesia until discharge from the post-anesthesia care unit in patients undergoing robotic-assisted surgery reduces perioperative oxygen desaturation and postoperative pulmonary complications.

Official title: Perioperative High-flow Nasal Oxygen in Patients Undergoing Robotic Surgery: A Randomized Trial

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

190

Start Date

2026-11-01

Completion Date

2029-10-31

Last Updated

2026-10-13

Healthy Volunteers

No

Conditions

Interventions

DEVICE

High flow nasal oxygen

In the intervention group, high-flow nasal oxygen (HFNO) will be initiated at the start of preoxygenation and maintained throughout the apneic phase of induction until successful tracheal intubation. HFNO will be reinitiated immediately prior to extubation and continued throughout the early postoperative period until discharge from the post-anesthesia care unit (PACU). HFNO can be discontinued earlier in the PACU at the discretion of the nurse treating the patient, or upon patient request. HFNO can further be changed to standard of care (standard oxygen mask or standard nasal cannula) at any time at the discretion of the anesthesia provider or PACU nurse. Flow rates and fraction of inspired oxygen (FiO₂) will follow the study protocol (60 liters per minute at 100% O2 for induction of anesthesia, 60 liters per minute at 70% O2 for extubation until 10 minutes after arrival in the PACU with subsequent weaning over the first hour after PACU arrival).

Locations (1)

Beth Israel Deaconess Medical Center

Boston, Massachusetts, United States