Nighttime tube removal: hidden danger for patients?
NCT ID NCT07752173
First seen Aug 07, 2026 · Last updated Aug 19, 2026 · Updated 3 times
Summary
This study asks whether removing a breathing tube (extubation) is riskier outside regular working hours. It will track thousands of adults undergoing surgery to compare complications like low oxygen or airway spasms during daytime versus evening/night shifts. The goal is to see if staff fatigue or reduced supervision plays a role, which could guide safer scheduling.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Extubation procedure and Karolinska Sleepiness Scale questionnaire
- What this could lead to
- If off-hours extubations prove riskier, hospitals could schedule staffing and supervision to reduce complications and improve patient safety.
- What could go wrong
- As an observational study, it can show associations but not prove cause. Results may be influenced by unmeasured factors like case complexity or staff experience.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 2,640 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Aug 2026
An estimate. Start dates often move.
- Expected to finish
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May 2027
An estimate. End dates often move.
- Lead sponsor
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A government agency
The lead sponsor is a government body.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
The study population comprises adult patients (aged ≥ 18 years, with no upper age limit) undergoing either elective or emergency surgery under general anaesthesia with endotracheal intubation at Kocaeli City Hospital, a tertiary referral centre in Turkey. Eligible participants are those in whom tracheal extubation is planned in the operating theatre or in the post-anaesthesia care unit (PACU). The population includes both American Society of Anesthesiologists (ASA) Class I-V patients, reflecting the full spectrum of surgical acuity and comorbidity burden encountered in routine clinical practice. Patients undergoing regional anaesthesia or sedation without intubation, those with a pre-existing tracheostomy, patients transferred intubated to the intensive care unit postoperatively, and those undergoing cardiothoracic surgery involving cardiopulmonary bypass are excluded. Additionally, patients requiring emergency airway management outside the operating theatre, those with a known or susp
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: \- Age ≥ 18 years Undergoing elective or emergency surgery under general anaesthesia with endotracheal intubation Planned tracheal extubation in the operating theatre or post-anaesthesia care unit (PACU) Provision of written informed consent (or deferred consent for emergency cases, in accordance with national regulations) Exclusion Criteria: * Patients undergoing surgery under regional anaesthesia or sedation without endotracheal intubation Patients with a tracheostomy in situ Patients who remain intubated and are transferred to the intensive care unit (ICU) postoperatively Patients undergoing cardiothoracic surgery involving cardiopulmonary bypass Emergency airway management performed outside the operating theatre (e.g., ICU, emergency department) Patients with known or suspected difficult airway requiring awake fibreoptic intubation Patients who refuse to provide informed consent or withdraw consent during the study Pregnant patients
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Kocaeli City Hospital
RECRUITINGKocaeli, Izmıt, 41001, Turkey (Türkiye)
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