🇮🇪Ireland
16°C Partly Cloudy · Dublin
Live Updates
--:--:-- IST
Contributor sign in
Latest
Clinical Trials in Turkey / NCT07484841
Recruiting Not applicable

Comparison of Awake Tracheal Intubation Methods

NCT07484841 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-03-20
Last updated
2026-08-26

Condition(s) studied

Airway Management AssessmentAwake Endotracheal IntubationAwake Fiberoptic Nasal IntubationVideolaryngoscopySupraglottic Airway Device Insertion

Investigational drug(s) / intervention(s)

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)

Awake tracheal intubation viaFiberoptic Bronchoscopy (ATI:FOB): awake tracheal intubation will be perform via FOB

Awake tracheal Intubation via videolaryngoscopy (ATI:VL): Awake tracheal intubation will be perform via videolaryngoscopy

awake tracheal intubation via aintree catheter loaded FOB through supraglottic airway device (ATI:SAD): Awake tracheal Intubation will be perform via aintree catheter loaded FOB through supraglottic airway device

Study summary

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.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
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

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Kocaeli City Hospital İzmit Kocaeli Recruiting

More Kocaeli City Hospital trials in Turkey

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07484841 on ClinicalTrials.gov ↗ ← All trials in Turkey