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NCT01936662 · ClinicalTrials.gov registry record · NA

Endotracheal Tube Versus Laryngeal Mask Airway for Esophagogastroduodenoscopy

A NA study, sponsored by Indiana University.

Completed
Registry status
NA
Development phase
84
Enrollment target

NCT01936662: Completed NA study, sponsored by Indiana University.

NCT01936662 is a NA study that has completed, run by Indiana University. The registered enrollment target is 84 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (94% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01936662, a NA study, has completed, sponsored by Indiana University.

COMPLETED
Registry status
NA
Development phase
84 participants
Enrollment target

Study Summary

Esophagogastroduodenoscopy (EGD) is a relatively common procedure in pediatric patients undergoing evaluation for various gastrointestinal ailments. The procedure itself, with or without associated biopsies, is relatively short in length. Unlike adults, who regularly undergo this procedure with conscious sedation, children most often require general anesthesia. While safe and effective, endotracheal tracheal tube (ETT) intubation of children for EGD can result in delayed awakening and slow room turnover, particularly when intravenous medications are required for intubation. Laryngeal mask airway (LMA) is an alternative to intubation, which permits removal before full awakening. Although considered a safe alternative to tracheal intubation in appropriate cases, disadvantages of the LMA have been reported including kinking, occluding view of the surgical field, failure of placement requiring tracheal intubation, aspiration of gastric contents, desaturation, and laryngospasm. The study was designed to determine whether use of an LMA for EGD could reduce operating room time, while providing satisfactory conditions for the endoscopist, and an equivalent side effect and safety profile as compared to ETT in otherwise healthy children with gastrointestinal complaints

Primary Outcome

Endoscopist was surveyed to determine their satisfaction with each of the airway devices. Endoscopist used the following satisfaction scale for each patient, regardless of the airway device used: 1. The airway device did not interfere at all with the ability to perform the scope. 2. The airway device presented some interference with the scope, but not enough to cause difficulty. 3. The airway device made it difficult to perform the endoscopy. 4. The airway device prevented the endoscopy from b

Interventions

  • DEVICE LMA
  • DEVICE ETT

Trial Details

FieldValue
Enrollment Target 84 participants
Start Date 2011-08
Est. Completion 2013-02
Phase NA
Indiana University

890 total trials

What the finished NCT01936662 record still lists

NCT01936662 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 84 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (94% lower).

The record links to 0 conditions, and to 2 interventions - of which LMA is the first listed.

NCT01936662 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01936662 about?

NCT01936662 is a clinical study titled "Endotracheal Tube Versus Laryngeal Mask Airway for Esophagogastroduodenoscopy". Esophagogastroduodenoscopy (EGD) is a relatively common procedure in pediatric patients undergoing evaluation for various gastrointestinal ailments. The procedure itself, with or without associated biopsies, is relatively short in length. Unlike adults, who regularly undergo this procedure with cons...

What is the current status of trial NCT01936662?

This trial is currently completed. It is a NA study. The enrollment target is 84 participants. The study started on 2011-08. Estimated completion is 2013-02.

What interventions are being tested in trial NCT01936662?

The interventions under investigation include: LMA (DEVICE), ETT (DEVICE).

Who is sponsoring clinical trial NCT01936662?

This trial is sponsored by Indiana University, which has 890 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01936662's enrollment target sits among peer trials

84 983rd of 2000 higher than 1,011 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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Source: ClinicalTrials.gov NCT01936662, the US trial registry maintained by the National Library of Medicine. NCT01936662 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.