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NCT Number: NCT06442930

EXtubation Related Complications - the EXTUBE Study (EXTUBE)

EXTUBE is an international, multicentre, prospective cohort study evaluating the incidence, risk factors, and outcomes of extubation-related complications and describing clinical practices related to extubation after general anesthesia or after critical illness in the operating room (OR), out of OR anesthesia location or intensive care unit (ICU).

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Key information

Conditions

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Royal North Shore Hospital, Sydney, New South Wales, Australia

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About this study

Globally, over 200 million people each year require extubation. While routinely performed, extubation is a skilled and potentially high-risk procedure that should be performed only when physiologic, pharmacologic, and contextual conditions are optimal. Complications at this stage of patient care can result in decreased oxygen delivery to the brain and body, sometimes leading to serious adverse events such as cardiac arrest, brain damage, or death. Indeed, one quarter of airway complications that result in death or brain death occur at the time of extubation.

Despite the frequency of extubation and the potential for life-threatening complications, there is a lack of systematic data on the rate and circumstances under which these severe complications occur. The limited data indicate 10-30% of extubations may lead to severe complications, depending on the population and outcome definition. However, the certainty of these estimates is severely limited because they are based on studies that are small, mostly single-center, based on clinician recall, only capture a small portion of extubation complications (e.g., malpractice claims), or do not reflect current clinical practice. In addition, most lack a denominator and exclude successful extubations, making estimates of actual complication rates and risk factors impossible.

There has been no large study of extubation techniques or adherence to guidelines, so procedural factors associated with complications must be elucidated. While adherence to clinical practice guidelines has not been formally evaluated, surveys show non-adherence to some best practices and considerable variation in practice, and data from audits and medicolegal claims show that lack of adherence to best practices is frequently at the root cause of severe adverse extubation outcomes, with half of the complications deemed preventable. Therefore, data on the frequency and nature of extubation complications, patient and procedural risk factors for complications, and guideline adherence rates are needed before these preventable events can be addressed.

EXTUBE (EXtubation related complications - an international observational study To Understand the impact and BEst practices in the operating room and intensive care unit) is an international, multicenter, prospective cohort study

The primary objective of this study is to estimate the incidence of immediate complications related to extubation in adult patients after general anesthesia and/or after critical illness. The secondary objectives are to determine: 1) the incidence of mild extubation complications; 2) patient- and procedure-related risk factors for extubation complications; 3) the association between extubation complications and outcomes until hospital discharge; and 4) the rate of adherence to extubation clinical practice guidelines.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adult patients (≥18 years old)
  • Undergoing extubation of an endotracheal tube (including index extubation and re-extubations) after general anesthesia in the OR, out of OR anesthesia location or ICU
  • Undergoing extubation during the specified enrollment window

Exclusion criteria

  • Patients will be excluded if the extubation is performed in the context of withdrawal of life support measures,
  • Patients will be excluded if the extubation is performed for tracheostomy decannulation

For each patient who is not included, reasons for exclusion will be reported.

Treatment and study plan

Primary outcomes

  1. At least one of the following, occurring within 60minutes after extubation (composite outcome): i) Severe hypoxemia ii) Cardiac arrest iii) Need for airway management

    Time frame: Within 60 minutes after the end of extubation

    The primary outcome will be the occurrence of at least one of the following (composite outcome) occurring within 60 minutes after the end of extubation:

    i) Severe hypoxemia (oxygen saturation as measured by pulse oximetry falls below SpO2 < 80% for > 5 minutes) ii) Cardiac arrest iii) Need for airway management (reintubation, insertion of a supraglottic airway, bag-mask ventilation).

Secondary outcomes

  1. Difficult airway and complications related to airway management if reintubation is required

    Time frame: Within 60 minutes after the end of extubation

    Difficult airway (i.e., experienced difficulty by an experienced airway manager with any or all of laryngoscopy or tracheal intubation, supraglottic airway use, face-mask ventilation, or front-of-neck airway) and complications related to airway management (e.g., esophageal intubation) if reintubation is required

  2. Planned and unplanned non-invasive respiratory support

    Time frame: Within 60 minutes after the end of extubation

    Planned and unplanned non-invasive respiratory support or high flow nasal cannula

  3. Emergency front of neck airway

    Time frame: Within 60 minutes after the end of extubation

    Emergency front of neck airway should airway management be required after extubation

  4. Cardiac arrhythmia requiring chemical or electrical treatment

    Time frame: Within 60 minutes after the end of extubation

    Cardiac arrhythmia requiring chemical or electrical treatment

  5. Severe Hypotension

    Time frame: Within 60 minutes after the end of extubation

    Severe hypotension (systolic arterial pressure < 65 mmHg recorded at any time or systolic arterial pressure < 90 mmHg for > 30 minutes or new need/increase of vasopressor and/or fluid load > 15 mL/kg)

  6. Severe Hypertension

    Time frame: Within 60 minutes after the end of extubation

    Severe hypertension (systolic blood pressure ≥180 mmHg and/or diastolic blood pressure ≥120 mmHg),

  7. Pulmonary aspiration

    Time frame: Within 60 minutes after the end of extubation

    Aspiration of gastric contents (gastric contents inhaled into the larynx and the respiratory tract)

  8. Barotrauma

    Time frame: Within 60 minutes after the end of extubation

    Pneumothorax/pneumo-mediastinum

  9. Dental injury

    Time frame: Within 60 minutes after the end of extubation

    Dental injury (notable change to the patient's dentition attributable to extubation or to reintubation, should this be required)

  10. Airways injury

    Time frame: Within 60 minutes after the end of extubation

    Airways injury (e.g., vocal cord damage, arytenoid dislocation

  11. Mortality

    Time frame: Within 7 days after extubation

    In-hospital mortality

  12. Re-intubation

    Time frame: Within 48 hours after extubation

    Re-intubation within 48 hours of extubation

Study contacts

Contact information is provided by the study sponsor or research team.

Matteo Parotto, MD, PhD

CONTACT

[email protected]

+1 416 340 3567

Shayan Wasim, MPH, BSc

CONTACT

[email protected]

+1 416 340 4800 ext. 4221

Sponsors and collaborators

Lead sponsor

University Health Network, Toronto

Other

Registry information

Official study title

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

Acronym: EXTUBE

Important dates

Study start
2025
Primary completion
2027
Study completion
2027
First posted
Jun 5, 2024
Registry last updated
Jul 21, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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