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Point of Care Ultrasound to Confirm Endotracheal Tube Cuff Position in Relationship to the Cricoid in Pediatric Population.

Senior Atending Anesthesiologist

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04479839
Enrollment
80
Registered
2020-07-21
Start date
2020-06-15
Completion date
2020-09-10
Last updated
2021-07-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cricoid Cartilage, Endotracheal Tube, Ultrasound

Brief summary

Anatomically, the infra-glottic area (subglottis) and the cricoid ring are the narrowest part of the larynx. In order to limit the incidence of damage related to mucosal pressure injuries from the presence of an endotracheal tube (ETT), the cuff of the ETT should lie below the cricoid in children. Previously, no clinical or imaging method has been used in real time at the bedside to determine the exact location of the ETT cuff after endotracheal intubation. Point-of-care ultrasound (POCUS) may provide an option for a safe and rapid means of visualizing the cuff of the ETT and its relationship to the cricoid ring in real-time thereby allowing ideal ETT positioning.

Detailed description

Airway below vocal cords until the distal end of the cricoid referred to as subglottis or infraglottis is considered to be the narrowest part of the airway. An optimal endotracheal tube (ETT) placement with cuffed ETT is to ensure the cuff position below the cricoid ring (cuff free glottis): as well have sufficient distance between ETT tip and carina. Various modalities including clinical examination, ETCO2, imaging (X-ray and ultrasound) are routinely used to verify the position and the tip of the ETT in the airway, however verification of the cuff position remains obscure.

Interventions

DIAGNOSTIC_TESTUltrasound of the airway

Placing ultrasound on the neck after intubation

Sponsors

Sidra Medicine
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
1 Days to 71 Months

Inclusion criteria

* Patients undergoing general anesthesia requiring endotracheal intubation

Exclusion criteria

* Patients with any anatomical airway deformity or mass

Design outcomes

Primary

MeasureTime frameDescription
Visualize the saline-filled cuff of the endotracheal tube3 monthsThe primary objective was to visualize the saline-filled cuff of the endotracheal tube in relation to the cricoid and tracheal rings

Countries

Qatar

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026