Actively Recruiting
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
Eligibility Criteria
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
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
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
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
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
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
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