Actively Recruiting

Age: 18Years +
All Genders
ID06442930

EXtubation Related Complications - an International Observational Study To Understand the Impact and BEst Practices in the Operating Room and Intensive Care Unit - the EXTUBE Study

Led by University Health Network, Toronto · Updated on 2026-06-03

3000

Participants Needed

30

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying extubation-related complications in adults who undergo extubation of an endotracheal tube after general anesthesia or critical illness. This international, multicenter observational study aims to estimate how often immediate complications occur, identify risk factors, assess outcomes up to hospital discharge, and evaluate adherence to clinical guidelines. Extubation can be risky, with serious events like cardiac arrest or brain damage possible, yet there is limited large-scale data on complication rates and practices. The study observes patients undergoing extubation in various settings including operating rooms, out-of-OR anesthesia locations, and intensive care units. It tracks complications and clinical practices without altering standard care. The research collects data on immediate events within 60 minutes after extubation, as well as outcomes like re-intubation and mortality within days. There are no experimental treatments; instead, the study focuses on monitoring and recording extubation-related events. Participants will have their extubation monitored for complications such as severe hypoxemia, cardiac arrest, airway issues, and more within one hour of extubation. Additional outcomes, including mortality up to seven days and re-intubation within 48 hours, will be recorded. The study also collects information on airway management difficulties and use of respiratory support. Data on adherence to extubation guidelines and patient outcomes will be analyzed. Participation duration varies, with enrollment during the specified study window and follow-up until hospital discharge or the defined outcome periods.

CONDITIONS

Brief Title

EXtubation Related Complications - the EXTUBE Study (EXTUBE)

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult patients (18 years old or older)
  • Undergoing extubation of an endotracheal tube after general anesthesia in the operating room, out of OR anesthesia location, or intensive care unit
  • Extubation occurs during the specified enrollment window
Not Eligible

You will not qualify if you...

  • Extubation performed in the context of withdrawal of life support measures
  • Extubation performed for tracheostomy decannulation

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Monitoring

Duration - Up to 60 minutes after extubation

Participants are observed during and immediately after extubation to record any complications and adherence to clinical practice guidelines.

1 visit during extubation and immediate post-extubation period

Long-term Monitoring

Duration - Up to 7 days after extubation

Participants are monitored for complications such as mortality and re-intubation occurring within days after extubation until hospital discharge.

Follow-up visits as part of routine care until hospital discharge

Trial Site Locations

Total: 30 locations

1

Banner University Medical Centre

Tucson, Arizona, United States, 85724-5114

Completed

2

University of Arkansas for Medical Sciences

Little Rock, Arkansas, United States, 72205

Completed

3

University of Florida

Gainesville, Florida, United States, 32608

Completed

4

The University of Chicago

Chicago, Illinois, United States, 60637

Actively Recruiting

5

Oregon Health & Science University

Portland, Oregon, United States, 97239

Completed

6

The University of Texas Health Science Center

Houston, Texas, United States, 77030

Completed

7

Royal North Shore Hospital

Sydney, New South Wales, Australia, 2065

Completed

8

The Northern Hospital

Melbourne, Victoria, Australia, 3076

Completed

9

Austin Hospital

Melbourne, Victoria, Australia, 3084

Completed

10

Eastern Health - Box Hill Hospital

Melbourne, Victoria, Australia, 3128

Completed

11

Eastern Health - Maroondah Hospital

Melbourne, Victoria, Australia, 3135

Completed

12

Eastern Health - Angliss Hospital

Melbourne, Victoria, Australia, 3156

Completed

13

Surrey Memorial Hospital

Surrey, British Columbia, Canada, V3V 1Z2

Completed

14

The Moncton Hospital

Moncton, New Brunswick, Canada, E1C 4B7

Completed

15

Sunnybrook Hospital

North York, Ontario, Canada, M4N 3M5

Completed

16

Niagara Health - Marotta Family Hospital

Saint Catharines, Ontario, Canada, L2S 0A9

Completed

17

St. Michael's Hospital

Toronto, Ontario, Canada, M5B 1W8

Completed

18

Mount Sinai Hospital

Toronto, Ontario, Canada, M5G 1X5

Completed

19

University Health Network - Toronto General Hospital

Toronto, Ontario, Canada, M5G 2C4

Completed

20

University Health Network - Toronto Western Hospital

Toronto, Ontario, Canada, M5T 2S8

Completed

21

Centre hospitalier de l'Université de Montréal (CHUM)

Montreal, Quebec, Canada, H2X 0C1

Completed

22

Mayo University Hospital

Castlebar, Ireland, F23 H529

Active, Not Recruiting

23

Cork University Hospital

Cork, Ireland, T12 DFK4

Completed

24

Mater Misericordiae University Hospital

Dublin, Ireland, D07 R2WY

Completed

25

Galway University Hospitals

Galway, Ireland, H91 YR71

Completed

26

Southland Hospital

Invercargill, New Zealand, 9812

Completed

27

Rotorua Hospital

Rotorua, New Zealand, 3010

Not Yet Recruiting

28

Tan Tock Seng Hospital

Singapore, Singapore, 308433

Completed

29

Royal United Hospitals Bath

Bath, United Kingdom, BA1 3NG

Completed

30

Freeman Hospital

Newcastle upon Tyne, United Kingdom, NE7 7DN

Completed

Loading map...

Research Team

M

Matteo Parotto, MD, PhD

S

Shayan Wasim, MPH, BSc

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

Similar Trials

Removal of the Intubation Tube Under Positive Pressure With ...

Mechanical Ventilation With Oral Intubation

Actively Recruiting

1 location

High Flow Nasal Cannula vs. Non-Invasive Ventilation in Post...

Heart Defects, Congenital

Actively Recruiting

1 location

Frequently Asked Questions

Have more questions? Get in touch with our team for quick support

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here