Tundra Space

Tundra Space

Clinical Research Directory

Browse clinical research sites, groups, and studies.

Back to Studies
RECRUITING
NCT05918575
NA

Postextubation Use of Noninvasive Respiratory Support in Severely Obese Patients

Sponsor: Rush University Medical Center

View on ClinicalTrials.gov

Summary

Around 20% of the obese patients with higher body mass index (BMI) who are taken off the breathing tube and breathing machine (ventilator) end up needing it back to support breathing. The re-application of breathing tube is associated with poor outcomes, including high risk of pneumonia, longer hospital stays, and death. The purpose of this study is to assess if prophylactic use of noninvasive breathing support after removing the breathing tube lowers the chance of needing the breathing tube again.

Official title: A Randomized Controlled Trial of Postextubation Use of Noninvasive Respiratory Support in Severely Obese Patients

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

250

Start Date

2023-07-10

Completion Date

2026-12-01

Last Updated

2025-10-20

Healthy Volunteers

No

Interventions

DEVICE

Noninvasive ventilation alternating with high flow nasal cannula

A total of 24 hours of prophylactic respiratory support will be provided using NIV alternating with HFNC with total NIV usage of 16 hours and HFNC usage of 8 hours.

DEVICE

High flow nasal cannula

A total of 24 hours of prophylactic respiratory support will be provided using HFNC alone.

Locations (5)

Rush University Medical Center

Chicago, Illinois, United States

Central DuPage Hospital

Winfield, Illinois, United States

McGovern Medical School, The University of Texas Health Science Center

Houston, Texas, United States

Medical College of Wisconsin

Milwaukee, Wisconsin, United States

Hospital Civil Fray Antonio Alcalde

Guadalajara, Jalisco, Mexico