Recruiting

Video Laryngoscopy vs. Direct Laryngoscopy

Sponsor:

Louisiana State University Health Sciences Center in New Orleans

Code:

NCT03775317

Conditions

Intubation, Intratracheal

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

Video Laryngoscopy

Direct Laryngoscopy

Study Details

Brief summary:

Nasotracheal intubation is a common method for securing an advanced airway during surgery for procedures that involve manipulation of the oral cavity, the dentition, or the facial bones. The placement of a nasotracheal tube is often more challenging, especially for learning providers, even for patients with normal airway anatomy. Video laryngoscopy is an adjunctive technique in anesthesia that utilizes a camera at the tip of the laryngoscope blade and provides an indirect view of the glottis during intubation through display on a monitor. The use of video laryngoscopes has been shown to reduce time to intubation, result in perception of easier intubation by the anesthesia team, and reduce the use of adjunctive maneuvers during intubation. There is little evidence, however, to show these benefits for routine nasotracheal intubation. The purpose of the study is to compare the ease of video-assisted laryngoscopy and direct laryngoscopy in routine nasotracheal intubation for Maxillofacial procedures. The investigators hypothesize that the use of video-assisted laryngoscopy for routine nasotracheal intubation will result in quicker time to intubation, less adjunctive maneuvers and anesthesia perception of easier intubation when compared to direct nasotrahceal intubation. The investigators aim to compare the time to intubation, number of adjunctive maneuvers and the perception of intubation difficulty in routine nasotracheal intubation for Maxillofacial procedures for video-assisted laryngoscopy and direct laryngoscopy.

Conditions

Intubation, Intratracheal

Study ID

NCT03775317

Start date

Dec 19, 2018

Status verified date

Mar, 2019

Completion date

Aug, 2019

Anticipated

Primary completion date

Jun, 2019

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • oral and maxillofacial surgery to be performed under general anesthesia
  • planned for a general anesthetic with nasotracheal intubation,
  • ASA I and II
  • at least 18 years of age

Exclusion Criteria:

  • prisoners
  • anticipated difficult airways

Study Design

Enrollment

50 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: Video Laryngoscopy

active comparator: Direct Laryngoscopy

Interventions

Video Laryngoscopy

The direct, or conventional, laryngoscopy group will undergo the planned nasotracheal intubation utilizing a Macintosh or Miller laryngoscope for direct visualization of the larynx.

Direct Laryngoscopy

The video-assisted laryngoscopy group will undergo the planned nasotracheal intubation utilizing a Storz C-MAC S Video Laryngoscope to allow for indirect visualization of the larynx.

Primary outcome measure

  • success of first attempt intubation [ Time Frame: 1 day ]

Central Contacts and Locations

Locations

University Medical Center

Recruiting

New Orleans, Louisiana, United States, 70112

Contacts

Principal Investigator:

Brett J King, DDS

More Information

Sponsor

Louisiana State University Health Sciences Center in New Orleans

Last update posted

Mar 15, 2019

Last verified

Mar, 2019

Keywords

  • Video laryngoscopy
  • Nasal intubation

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Louisiana State University Health Sciences Center in New Orleans on 2019-03-15.