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Utilization of Airway Stabilizing Rod

Utilization of Airway Stabilizing Rod to Assist With LMA Guided Fiberoptic Intubation in Children

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05899868
Acronym
FASTER
Enrollment
20
Registered
2023-06-12
Start date
2023-10-12
Completion date
2024-05-17
Last updated
2024-12-05

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

Conditions

Airway Complication of Anesthesia

Brief summary

The pediatric airway is known to be more challenging than the adult airway when performing endotracheal intubation. When a patient cannot be ventilated and/or intubated, the guidelines for airway management dictate that a laryngeal mask airway (LMA) be used as a rescue device to oxygenate and ventilate the patient. While an excellent device the LMA is seen as temporary and ultimately needs to be replaced by an endotracheal tube (ETT).

Detailed description

The objective is to study this device in patients with difficult airway to assess the success rate and time to intubation for placing an endotracheal tube using this device.

Interventions

DEVICETime to Intubation using FASTER device

Time from fiberoptic placement onto airway to documentation of end-tidal carbon dioxide waveform through the endotracheal tube.

Sponsors

Baylor College of Medicine
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DEVICE_FEASIBILITY
Masking
NONE

Intervention model description

Testing of device for success during endotracheal intubation

Eligibility

Sex/Gender
ALL
Age
5 Years to 18 Years
Healthy volunteers
No

Inclusion criteria

* Ages 5-18 years * Requiring intubation * Known difficult airway * LMA placement possible

Exclusion criteria

* Known normal airway * Procedure not requiring endotracheal intubation * Parental refusal * Patient dissent

Design outcomes

Primary

MeasureTime frameDescription
Overall time in the airway5 minutesTime from fiberoptic placement onto airway to documentation of end-tidal carbon dioxide waveform through the endotracheal tube.
Total time to intubation3 minutesTime from movement of the device to documentation of end-tidal carbon dioxide waveform through the endotracheal tube.

Countries

United States

Outcome results

None listed

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