Hybrid Intubation Technique for Difficult Airway Children

Sponsor
Seoul National University Hospital (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06058221
Collaborator
(none)
116
2
22

Study Details

Study Description

Brief Summary

To compare two hybrid techniques, flexible bronchoscopy-guided intubation with a video laryngoscope and flexible bronchoscopy-guided intubation with a laryngeal mask, that have recently shown promise as a way to increase first-attempt success rates and reduce complications in children with anticipated difficult intubation.

Condition or Disease Intervention/Treatment Phase
  • Device: simultaneous videolaryngoscopy
  • Device: supraglottic airway
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
116 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Prevention
Official Title:
Fiberoptic Intubation With Simultaneous Video-laryngoscopy Versus Through a Supraglottic Airway in Children With a Difficult Airway: a Randomized Controlled Trial
Anticipated Study Start Date :
Oct 1, 2023
Anticipated Primary Completion Date :
Jul 31, 2025
Anticipated Study Completion Date :
Jul 31, 2025

Arms and Interventions

Arm Intervention/Treatment
Experimental: Hybrid technique

Device: simultaneous videolaryngoscopy
Two specialists perform tracheal intubation, one using a video laryngoscope to expose the vocal cords and the other using a fiberoptic bronchoscope.

Active Comparator: Supraglottic airway

Device: supraglottic airway
After inserting the supraglottic airway, the specialist performs intubation using a fiberoptic bronchoscope through the supraglottic airway.

Outcome Measures

Primary Outcome Measures

  1. first attempt intubation success rate [from induction of anesthesia to 1 minutes after intubation, about 10 minutes.]

    The success rate of a healthcare provider's first attempt to insert a tube into a patient's airway. Intubation is defined as successful if the tube is inserted and capnography is first seen. If the fiberoptic bronchoscope comes out of the mouth, it is a failure.

Secondary Outcome Measures

  1. total intubation time (seconds) [from induction of anesthesia to 1 minutes after intubation, about 10 minutes.]

    Time from when the performer ends mask ventilation to when capnography first appears.

  2. Number of intubation attempts [from induction of anesthesia to 1 minutes after intubation, about 10 minutes.]

    Total number of attempts to intubate, regardless of the method used (failures include bronchoscopy out of the mouth, videolaryngoscope or supraglottic airway out of the mouth, or retrying manual ventilation, even if the method is the same).

  3. successful tracheal intubation with the allocated method [from induction of anesthesia to 1 minutes after intubation, about 10 minutes.]

    Whether successful in intubation according to the allocated method or not

  4. successful tracheal intubation (Yes or No) [from induction of anesthesia to 1 minutes after intubation, about 10 minutes.]

    To define and confirm that "successful intubation" occurs when the endotracheal tube is successfully placed inside the trachea, capnography is visible, and surgery can proceed as a result of successful endotracheal intubation.

  5. Nadir oxygen saturation during intubation (SpO2 value, %) [from induction of anesthesia to 1 minutes after intubation, about 10 minutes.]

    the minimum oxygen saturation reported during intubation periods

  6. Oxygen reserve index during intubation (ORi™, Rainbow Signal Extraction Technology) [from induction of anesthesia to 1 minutes after intubation, about 10 minutes.]

    the trends of oxygen reserve index during intubation period per 5 seconds

  7. intubation-related complication [from induction of anesthesia to 1 minutes after intubation, about 10 minutes.]

    Complications associated with intubation (airway injury, esophageal intubation, laryngospasm, bronchospasm, intraoral bleeding, arrhythmia, cardiac arrest).

  8. The degree of vocal cord exposure assessed with a flexible bronchoscope. (Modified Cormack-Lehane grade, I/II/III/IV) [from induction of anesthesia to 1 minutes after intubation, about 10 minutes.]

    Degree of vocal cord exposure, as determined by the Modified Cormack-Lehane grade, when a flexible bronchoscope is inserted by the anesthesiologist.

Eligibility Criteria

Criteria

Ages Eligible for Study:
1 Month to 12 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Children from 1 month of age to less than 12 years of age who are expected to have a difficult intubation when undergoing routine surgery under general anesthesia.
Exclusion Criteria:
  • When there is limited mouth opening, making it difficult to insert supraglottic airway ② The patient or their parents do not agree to participate in the study. ③ Other cases deemed unsuitable by the researcher

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Seoul National University Hospital

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Eun-hee Kim, Clinical Associate Professor, Seoul National University Hospital
ClinicalTrials.gov Identifier:
NCT06058221
Other Study ID Numbers:
  • H-2308-024-1457
First Posted:
Sep 28, 2023
Last Update Posted:
Sep 28, 2023
Last Verified:
Sep 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Sep 28, 2023