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NCT03032263 · ClinicalTrials.gov registry record · NA
Video vs. Direct Laryngoscopy in Pediatric Nasal Intubation
A NA study, sponsored by Wake Forest University Health Sciences.
- Terminated
- Registry status
- NA
- Development phase
- 12
- Enrollment target
NCT03032263: Clinical Trial NA study, sponsored by Wake Forest University Health Sciences.
NCT03032263 is a NA study that was terminated before completion, run by Wake Forest University Health Sciences. The registered enrollment target is 12 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT03032263, a NA study, was terminated before completion, sponsored by Wake Forest University Health Sciences.
- TERMINATED
- Registry status
- NA
- Development phase
- 12 participants
- Enrollment target
Study Summary
Nasal intubation is frequently used for dental procedures to promote an unimpeded view of the oral cavity. A nasal RAE endotracheal tube is longer than a standard oral endotracheal tube (ETT) and it is shaped so that end of the tube which attaches to the ventilator exits upward toward the forehead. This unique shape ensures that the tube will not interfere with surgical exposure of the oral cavity and mandible. The nasal RAE ETT can be placed in the trachea using either direct laryngoscopy (DL) or video laryngoscopy (C-Mac) . Sometimes this is possible without an adjuvant, but frequently a pair of specially shaped forceps, known as Magill forceps, is required to guide the distal tip of the Nasal RAE into the glottis due to the curvature of these ETT. Magill forceps are introduced into the mouth and are used to grasp the distal end of the Nasal RAE and direct it into the glottis. Contrary to what the current literature suggests, it has been our experience that nasal intubations using the C-Mac frequently do not require the use of Magill forceps at nearly the same rate as DL. This technique may improve the time and ease to intubation because of not having to use the Magill forceps. The use of Magill forceps can be awkward for the clinician, with poor visualization due to obstruction of the view by this tool in the airway, and small working space within the posterior oropharynx. For these reasons, the possibility of not having to use Magill forceps because the investigators are using a C-Mac as the only tool to intubate is a potentially inviting one.
Primary Outcome
Reported as the number and percentage of participants that needed the use of Magill forceps during intubation
Interventions
- DEVICE Direct Laryngoscopy
- DEVICE Video Laryngoscopy for nasal intubation
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 12 participants |
| Start Date | 2016-03 |
| Est. Completion | 2017-08-07 |
| Phase | NA |
Why NCT03032263 stopped before completion
NCT03032263 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 12 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).
The record links to 0 conditions, and to 2 interventions - of which Direct Laryngoscopy is the first listed.
NCT03032263 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT03032263 about?
NCT03032263 is a clinical study titled "Video vs. Direct Laryngoscopy in Pediatric Nasal Intubation". Nasal intubation is frequently used for dental procedures to promote an unimpeded view of the oral cavity. A nasal RAE endotracheal tube is longer than a standard oral endotracheal tube (ETT) and it is shaped so that end of the tube which attaches to the ventilator exits upward toward the forehead. ...
What is the current status of trial NCT03032263?
This trial is currently terminated. It is a NA study. The enrollment target is 12 participants. The study started on 2016-03. Estimated completion is 2017-08-07.
What interventions are being tested in trial NCT03032263?
The interventions under investigation include: Direct Laryngoscopy (DEVICE), Video Laryngoscopy for nasal intubation (DEVICE).
Who is sponsoring clinical trial NCT03032263?
This trial is sponsored by Wake Forest University Health Sciences, which has 1,140 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT03032263's enrollment target sits among peer trials
12 1913th of 2000 higher than 74 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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