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Trial · NCT07902986

Registered outcomes11

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryModified Cormack-Lehane Grade in the Sniffing Position Versus the LeHeR PositionDuring direct laryngoscopy, approximately 3-10 minutes after induction of general anesthesia
Glottic view obtained during direct laryngoscopy with a Macintosh blade, graded using the modified Cormack-Lehane classification (1, 2A, 2B, 3A, 3B, 4; higher grades indicate a worse view). Each patient is assessed first in the sniffing position and then after 45° left head rotation (LeHeR), and the paired grades are compared within the same patient.
PrimaryPercentage of Glottic Opening (POGO) Score in the Sniffing Position Versus the LeHeR PositionDuring direct laryngoscopy, approximately 3-10 minutes after induction of general anesthesia
Percentage (0-100%) of the glottic opening visible from the anterior commissure to the interarytenoid notch during direct laryngoscopy; higher values indicate a better view. Each patient is assessed first in the sniffing position and then after 45° left head rotation (LeHeR), and the paired scores are compared within the same patient.
SecondaryIntubation Difficulty Scale (IDS) ScoreDuring endotracheal intubation, from first laryngoscopy until confirmed tracheal intubation
IDS score calculated as the sum of seven parameters (N1-N7): number of additional attempts, number of additional operators, number of alternative techniques, Cormack-Lehane grade minus 1 in the position in which intubation is achieved, increased lifting force (0/1), need for external laryngeal pressure (0/1), and vocal cord position (abducted 0 / adducted 1). Score 0 = easy intubation, 1-5 = slight difficulty, \>5 = moderate to major difficulty.
SecondaryEase of IntubationDuring endotracheal intubation, from first laryngoscopy until confirmed tracheal intubation
Ease of intubation categorized as: easy (successful at first attempt without additional maneuvers), moderate (successful at first attempt with additional maneuvers such as external laryngeal manipulation or stylet/bougie, or at second attempt), difficult (more than two attempts, a different operator or a different technique required, but ultimately successful), or impossible (fiberoptic/awake intubation required or failed intubation).
SecondaryNumber of Participants Requiring Additional Airway ManeuversDuring endotracheal intubation, from first laryngoscopy until confirmed tracheal intubation
Number of participants requiring BURP (backward-upward-rightward pressure), external laryngeal manipulation, or return of the head to the sniffing position to achieve intubation after the LeHeR maneuver.
SecondaryNumber of Participants Requiring a Bougie or StyletDuring endotracheal intubation, from first laryngoscopy until confirmed tracheal intubationNumber of participants in whom a gum elastic bougie or stylet is required to achieve endotracheal intubation.
SecondaryIntubation TimeDuring endotracheal intubation, from first laryngoscopy until confirmed tracheal intubationTime in seconds from passage of the laryngoscope blade between the lips to the appearance of the first end-tidal carbon dioxide waveform on capnography.
SecondaryNumber of Participants With Airway TraumaFrom first laryngoscopy until 5 minutes after intubationNumber of participants with signs of airway trauma, defined as blood on the laryngoscope blade or endotracheal tube, or lip, dental or oropharyngeal mucosal injury.
SecondaryHeart RateBaseline (before induction), after induction, and at 1, 3, 5 and 10 minutes after intubationHeart rate (beats/min) recorded at predefined time points to assess hemodynamic and oxygenation changes associated with laryngoscopy and intubation.
SecondaryMean Arterial PressureBaseline (before induction), after induction, and at 1, 3, 5 and 10 minutes after intubationMean arterial pressure (mmHg) recorded at predefined time points to assess hemodynamic and oxygenation changes associated with laryngoscopy and intubation.
SecondaryPeripheral Oxygen SaturationBaseline (before induction), after induction, and at 1, 3, 5 and 10 minutes after intubationPeripheral oxygen saturation (SpO2, %) recorded at predefined time points to assess hemodynamic and oxygenation changes associated with laryngoscopy and intubation.

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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