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- Registre américain des essais cliniques
- Essai clinique NCT07752173
Comparison of Acute Airway/Respiratory Complications and Intervention Requirements in Extubations Performed During On-Hours Versus Off-Hours
Comparison of Acute Airway/Respiratory Complications and Intervention Requirements in Extubations Performed During On-Hours Versus Off-Hours: A Prospective Observational Cohort Study
Aperçu de l'étude
Statut
Intervention / Traitement
Description détaillée
Type d'étude
Inscription (Estimé)
Contacts et emplacements
Coordonnées de l'étude
- Nom: Mehmet Yilmaz, Md
- Numéro de téléphone: 05052174432
- E-mail: drmyilmaz33@gmail.com
Sauvegarde des contacts de l'étude
- Nom: Ali Mete Temel, Md
- Numéro de téléphone: +905438465215
- E-mail: metetemel60@hotmail.com
Lieux d'étude
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Izmıt
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Kocaeli, Izmıt, Turquie (Türkiye), 41001
- Recrutement
- Kocaeli City Hospital
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Contact:
- Mehmet Yilmaz, Md
- Numéro de téléphone: 05052174432
- E-mail: drmyilmaz33@gmail.com
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Sous-enquêteur:
- Mehmet Yilmaz, Md
-
Contact:
- Ali Mete Temel, Md
- Numéro de téléphone: +905438465215
- E-mail: metetemel60@hotmail.com
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Chercheur principal:
- Ali Mete Temel, Md
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-
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
- Adulte plus âgé
Accepte les volontaires sains
Méthode d'échantillonnage
Population étudiée
La description
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
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
Cohortes et interventions
Groupe / Cohorte |
Intervention / Traitement |
|---|---|
|
On-Hours
On-hours group: Extubations performed between 08:00 and 16:00 on weekdays (Monday to Friday), excluding public holidays.
|
An extubation attempt is the planned, deliberate removal of the endotracheal tube from the patient's trachea, beginning with preparatory manoeuvres (such as oropharyngeal suctioning and cuff deflation) and ending with the complete withdrawal of the tube and establishment of a patent native airway with adequate spontaneous breathing.
Description: The Karolinska Sleepiness Scale (KSS), a validated 9-point Likert scale (1 = extremely alert, 9 = very sleepy, fighting sleep), will be administered to the attending anaesthetist responsible for performing the extubation immediately prior to the extubation procedure.
This assessment is performed to objectively quantify the clinician's subjective level of sleepiness and fatigue at the time of extubation.
The KSS score will be recorded as a predictor/exposure variable to evaluate the association between anaesthetist fatigue and the occurrence of acute airway and respiratory complications during extubation.
This assessment is applied uniformly across both study groups (on-hours and off-hours extubations).
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|
Off-Hours
Off-hours group: Extubations performed after 16:00 on weekdays, as well as all extubations performed on weekends and public holidays, regardless of the time of day
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An extubation attempt is the planned, deliberate removal of the endotracheal tube from the patient's trachea, beginning with preparatory manoeuvres (such as oropharyngeal suctioning and cuff deflation) and ending with the complete withdrawal of the tube and establishment of a patent native airway with adequate spontaneous breathing.
Description: The Karolinska Sleepiness Scale (KSS), a validated 9-point Likert scale (1 = extremely alert, 9 = very sleepy, fighting sleep), will be administered to the attending anaesthetist responsible for performing the extubation immediately prior to the extubation procedure.
This assessment is performed to objectively quantify the clinician's subjective level of sleepiness and fatigue at the time of extubation.
The KSS score will be recorded as a predictor/exposure variable to evaluate the association between anaesthetist fatigue and the occurrence of acute airway and respiratory complications during extubation.
This assessment is applied uniformly across both study groups (on-hours and off-hours extubations).
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Incidence of Desaturation During Extubation
Délai: 30 min. after extubation
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Description: The occurrence of desaturation during the extubation procedure itself, defined as a peripheral oxygen saturation (SpO₂) < 90% lasting for ≥ 30 seconds (or a ≥ 5% decrease from baseline in patients with pre-existing hypoxaemia), measured from the initiation of extubation manoeuvres (cuff deflation and suctioning) until the complete withdrawal of the endotracheal tube. Time Frame: Desaturation occurring during the extubation attempt and within the first 30 minutes post-extubation. |
30 min. after extubation
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Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Other acute airway/respiratory complications
Délai: 30 min. after extubation
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(laryngospasm, airway obstruction, bronchospasm, aspiration, apnoea, haemodynamic instability, arrhythmias, unplanned reintubation, surgical airway).
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30 min. after extubation
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Autres mesures de résultats
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Intervention requirement by type
Délai: 30 min. after extubation
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(simple airway manoeuvres, bag-mask ventilation, pharmacological agents, reintubation, surgical airway)
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30 min. after extubation
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Collaborateurs et enquêteurs
Parrainer
Les enquêteurs
- Chaise d'étude: Mehmet Yilmaz, Kocaeli City Hospital
Publications et liens utiles
Publications générales
- Xie Q, Shen Z, Pan M, Li Y, Luo Z, Wang C, Zhao L, Fang Y, Ding X, Teng J, Xu J. Weekend effect on the incidence and outcomes of cardiac surgery associated - acute kidney injury. BMC Cardiovasc Disord. 2023 Oct 27;23(1):524. doi: 10.1186/s12872-023-03431-4.
- Patel MS, Thomas JJ, Aguayo X, Gutmann D, Sarwary SH, Wain M. The Effect of Weekend Surgery on Outcomes of Emergency Laparotomy: Experience at a High Volume District General Hospital. Cureus. 2022 Mar 27;14(3):e23537. doi: 10.7759/cureus.23537. eCollection 2022 Mar.
- Ash-Rafzadeh H, Chambers TJ, Velez FO, Moodie CC, Garrett JR, Fontaine JP, Toloza EM. Effect of Surgical Day of Week on Postoperative Outcomes After Robotic-Assisted Pulmonary Lobectomy. Cureus. 2023 Feb 23;15(2):e35379. doi: 10.7759/cureus.35379. eCollection 2023 Feb.
- Maman D, Steinfeld Y, Berkovich Y. No Weekend Effect in Elective Primary Total Knee Arthroplasty: A Nationwide Analysis of 437,121 U.S. Cases. J Clin Med. 2025 Dec 12;14(24):8816. doi: 10.3390/jcm14248816.
- Cortegiani A, Gregoretti C, Neto AS, Hemmes SNT, Ball L, Canet J, Hiesmayr M, Hollmann MW, Mills GH, Melo MFV, Putensen C, Schmid W, Severgnini P, Wrigge H, Gama de Abreu M, Schultz MJ, Pelosi P; LAS VEGAS Investigators, the PROVE Network, and the Clinical Trial Network of the European Society of Anaesthesiology. Association between night-time surgery and occurrence of intraoperative adverse events and postoperative pulmonary complications. Br J Anaesth. 2019 Mar;122(3):361-369. doi: 10.1016/j.bja.2018.10.063. Epub 2019 Feb 8.
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Estimé)
Achèvement primaire (Estimé)
Achèvement de l'étude (Estimé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Mots clés
Termes MeSH pertinents supplémentaires
- Qualité des soins de santé, accès et évaluation
- Techniques d'investigation
- Méthodes épidémiologiques
- Thérapeutique
- Collecte de données
- Mécanismes d'évaluation des soins de santé
- Qualité des soins de santé
- Santé publique
- Environnement et santé publique
- Gestion des voies respiratoires
- Enquêtes et questionnaires
- Extubation des voies respiratoires
Autres numéros d'identification d'étude
- KSH-2026-89
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
Description du régime IPD
Informations sur les médicaments et les dispositifs, documents d'étude
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