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NCT Number: NCT07004998

PARAtracheal vs CRIcoid Pressure on GLIttic DEformation (PARAGLIDE)

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.

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Key information

Conditions

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age ≥ 18 years
  • Scheduled for elective surgery under general anesthesia requiring endotracheal intubation
  • ASA physical status I or II
  • Normal airway anatomy as assessed by the anesthesiologist (Mallampati I-II, no known or anticipated difficult airway)
  • Written informed consent obtained prior to inclusion

Exclusion criteria

  • History of difficult intubation or anticipated difficult airway
  • Known upper airway anatomical abnormalities (e.g., tumors, tracheal deviation, cervical spine instability)
  • BMI > 35 kg/m²
  • Gastroesophageal reflux disease or increased aspiration risk
  • Pregnancy
  • Emergency surgery
  • Allergy or contraindication to any anesthetic drugs used
  • Inability to provide informed consent

Treatment and study plan

Cricoid Pressure (30 N)

Procedure

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

Left Paratracheal Pressure (30 N)

Procedure

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

Primary outcomes

  1. Percentage of Glottic Opening (POGO) score

    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%).

Secondary outcomes

  1. Glottic surface area

    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.

  2. Vertical Displacement of the Glottic Plane

    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.

  3. Horizontal displacement of the glottic plane

    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.

  4. First-pass intubation success

    Time frame: From laryngoscope insertion to first confirmed capnography

    Successful tracheal intubation at the first attempt with the maneuver chosen by the operator.

  5. Time to intubation

    Time frame: From laryngoscope insertion to first confirmed capnography

    Duration in seconds until successful tracheal intubation.

  6. Intubation Difficulty Scale (IDS)

    Time frame: During intubation

    Composite score including attempts, operators, optimization maneuvers, and force required.

  7. First-attempt success without desaturation < 90%

    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.

  8. Hypoxemia

    Time frame: From induction until confirmed intubation

    Oxygen saturation <92% recorded by pulse oximetry.

  9. Hemodynamic events

    Time frame: From induction until confirmed intubation

    Systolic blood pressure drop >20% from baseline or heart rate <50/min.

  10. Airway trauma

    Time frame: Immediately after intubation

    Blood on blade/stylet or visible lip/mucosal injury.

  11. Postoperative sore throat

    Time frame: 30-60 minutes in PACU

    Patient-reported throat pain on numeric scale (0-10).

Study contacts

Contact information is provided by the study sponsor or research team.

Benjamin Javillier, M.D.

CONTACT

[email protected]

081209155 ext. +32

Sponsors and collaborators

Lead sponsor

University of Liege

Other

Registry information

Official study title

Comparison of Left Paratracheal Versus Cricoid Pressure on Glottic Visualization During Videolaryngoscopy: A Randomized Crossover Study

Acronym: PARAGLIDE

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
Jun 4, 2025
Registry last updated
Sep 19, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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