Clinique Saint-Luc
Bouge, Namur, Belgium
NCT Number: NCT07004998
This randomized crossover study evaluates the effects of left paratracheal pressure, cricoid pressure, and no pressure on glottic visualization during videolaryngoscopy in adult surgical patients. The primary endpoint is the Percentage of Glottic Opening (POGO) score assessed by blinded video review. Secondary endpoints include anatomical measures (glottic surface area, vertical and horizontal displacement of the glottic plane) and clinical outcomes (first-pass success, first-pass success without desaturation <90%, intubation time, Intubation Difficulty Scale, hypoxemia, hemodynamic events, airway trauma, and postoperative sore throat or dysphonia). All outcomes are collected from routine anesthetic practice and video analysis, with no additional procedures.
Trial opening soon.
Get Notified18 year and older
All sexes
Interventional
Not applicable
Bouge, Namur, Belgium
This randomized crossover trial will compare three laryngoscopy conditions (no pressure, cricoid pressure, left paratracheal pressure) in adult surgical patients requiring general anesthesia with tracheal intubation. Each patient undergoes all three conditions in random order, with the intubation performed using the maneuver chosen by the operator. Anatomical outcomes (POGO, glottic surface area, vertical and horizontal displacement of the glottic plane) will be assessed from video recordings by blinded evaluators. Clinical outcomes (first-pass success, composite success without desaturation <90%, intubation time, IDS, hypoxemia, hemodynamic changes, airway trauma, sore throat, dysphonia) will be collected from routine anesthetic records and PACU assessments.
Statistical Analysis Plan:
POGO: mixed-effects repeated measures model with patient as random effect, maneuver as fixed effect, adjusted for operator, BMI, and Mallampati.
Anatomical outcomes: analyzed similarly with mixed models and planned contrasts (LPP vs CP).
Clinical outcomes: analyzed as-treated, using logistic or linear regression with adjustments for baseline factors and operator as random effect.
Mediation analysis will evaluate whether improvements in POGO explain clinical benefits (first-pass success, intubation time).
Significance level set at α=0.05 (two-sided), with exploratory outcomes interpreted without multiplicity correction.
Missing data (e.g., unusable videos, missing sore throat scores) will be reported; complete-case analysis will be primary, sensitivity analysis considered if >5% missing.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Manual application of posterior pressure on the cricoid cartilage at a standardized force of 30 newtons. The pressure is applied by a trained operator using one or two fingers, with the goal of compressing the esophagus against the cervical spine. The maneuver is performed after induction of general anesthesia and immediately before videolaryngoscopy. A still image of the glottic view is captured during pressure application.
Other names: Sellick Maneuver, Cricoid Force, CP, Cricoid Compression, Cricoid Pressure
Manual application of pressure to the left paratracheal region, lateral to the trachea and inferior to the thyroid cartilage, at a standardized force of 30 newtons. The pressure is applied by a trained operator using the thumb or fingers. The maneuver is performed after induction of general anesthesia and immediately before videolaryngoscopy. A still image of the glottic view is captured during pressure application.
Other names: LPP, Left Paratracheal Pressure
Time frame: During laryngoscopy, before tracheal intubation
POGO will be scored from video recordings of each condition (no pressure, cricoid, paratracheal) by blinded assessors (0-100%).
Time frame: During laryngoscopy, before intubation
Glottic surface area will be quantified from videolaryngoscopic images under each condition (no pressure, cricoid, paratracheal) using standardized image analysis by blinded reviewers.
Time frame: During laryngoscopy, before intubation
The vertical shift of the glottic plane relative to baseline will be measured on recorded videolaryngoscopic images under each condition, assessed by blinded reviewers.
Time frame: During laryngoscopy, before intubation
The horizontal (lateral) shift of the glottic plane relative to baseline will be measured on recorded videolaryngoscopic images under each condition, assessed by blinded reviewers.
Time frame: From laryngoscope insertion to first confirmed capnography
Successful tracheal intubation at the first attempt with the maneuver chosen by the operator.
Time frame: From laryngoscope insertion to first confirmed capnography
Duration in seconds until successful tracheal intubation.
Time frame: During intubation
Composite score including attempts, operators, optimization maneuvers, and force required.
Time frame: From laryngoscope blade past the incisors until confirmed tracheal intubation (end-tidal CO₂ ≥ 5 mmHg for 3 breaths), typically up to 2 minutes.
Binary composite. Success = both (1) first-attempt intubation (tube placed without complete blade removal; optimizations allowed without blade withdrawal) and (2) no SpO₂ < 90% for ≥ 5 s within the time frame.
Time frame: From induction until confirmed intubation
Oxygen saturation <92% recorded by pulse oximetry.
Time frame: From induction until confirmed intubation
Systolic blood pressure drop >20% from baseline or heart rate <50/min.
Time frame: Immediately after intubation
Blood on blade/stylet or visible lip/mucosal injury.
Time frame: 30-60 minutes in PACU
Patient-reported throat pain on numeric scale (0-10).
Contact information is provided by the study sponsor or research team.
University of Liege
Other
Comparison of Left Paratracheal Versus Cricoid Pressure on Glottic Visualization During Videolaryngoscopy: A Randomized Crossover Study
Acronym: PARAGLIDE
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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