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โ† Trials
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Comparison of Awake Tracheal Intubation Methods

RecruitingNAAges 18 Years - anyAllKocaeli City Hospital
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In plain words

What the trial is, and whether it could suit you

The aim of this study was to compare three different awake tracheal intubation technique -fiberoptic bronchoscopy (ATI:FB), videolaryngoscopy (ATI:VL), and fiberoptic bronchoscopy via a supraglottic airway device (ATI:SAD)- in terms of success rates, intubation times, and complications. Additionally, the study aims to evaluate the reliability of the SAD-assisted ATI method and its potential to contribute to the literature.

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๐Ÿ“‹ Eligibility rules (as published)
Inclusion Criteria: * Adult patients aged 18 and older * Patients classified as ASA I-II according to the American Society of Anesthesiologists (ASA) classification * Patients scheduled for elective surgery * Patients expected to require difficult mask ventilation, difficult laryngoscopy, or difficult tracheal intubation; patients expected to have short apnea periods (Planjuan goiter); patients at risk of aspiration; patients expected to require difficult rescue techniques; and patients with a reported history of difficult intubation * Patients scheduled for intubation using the awake tracheal intubation (ATI) method * Individuals who have agreed to participate in the study by signing an informed consent form Exclusion Criteria: * Patients with a mouth opening \<1.5 cm * Patients requiring emergency intubation or emergency surgery (situations where there is insufficient time to administer ATI) * Patients who cannot cooperate (mental incapacity, impaired consciousness, inability to communicate, etc.) * Patients with known allergies to lidocaine or other local/topical anesthetic agents used * Pregnancy * Patients with a history of severe cardiac arrhythmia or hemodynamic instability (due to increased risk during intubation) * Patients who have previously undergone tracheostomy or whose airway is technically obstructed due to anatomical deformity * Patients who refuse to participate in the study or who do not provide informed consent
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What it tests

  • Awake tracheal intubation viaFiberoptic Bronchoscopy (ATI:FOB)
  • Awake tracheal Intubation via videolaryngoscopy (ATI:VL)
  • awake tracheal intubation via aintree catheter loaded FOB through supraglottic airway device (ATI:SAD)
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Where

1 site
Kocaeli City Hospital
ฤฐzmit, Turkey (Tรผrkiye)
๐Ÿค Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible โ€” always decide together with your own doctor.
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