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NCT01633073 · ClinicalTrials.gov registry record · NA

A Comparison of the Laryngeal Mask Airway (LMA) Supreme and I-gel in Children

A NA study, sponsored by Ann & Robert H Lurie Children's Hospital of Chicago.

Completed
Registry status
NA
Development phase
170
Enrollment target

NCT01633073 is a NA study that has completed, run by Ann & Robert H Lurie Children's Hospital of Chicago. The registered enrollment target is 170 participants.

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The verdict

NCT01633073, a NA study, has completed, sponsored by Ann & Robert H Lurie Children's Hospital of Chicago.

COMPLETED
Registry status
NA
Development phase
170 participants
Enrollment target

Study Summary

The aim of this randomized prospective study is to compare two single-use laryngeal mask airways with a provision of a gastric drain tube allowing for evacuation of gastric contents, the i-gel and the LMA Supreme, in pediatric patients undergoing positive pressure ventilation. The investigators hypothesize that airway leak pressures with the i-gel will not be significantly different clinically (higher) when compared with the LMA Supreme.

Interventions

  • DEVICE LMA Supreme: control device
  • DEVICE i-gel: comparison device

Trial Details

FieldValue
Enrollment Target 170 participants
Start Date 2012-06
Est. Completion 2012-09
Phase NA

What the Registry Record Tells You About NCT01633073

The ClinicalTrials.gov registry entry for NCT01633073 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 170 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Ann & Robert H Lurie Children's Hospital of Chicago, which has 159 total studies on file at ClinicalTrials.gov.

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

NCT01633073 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01633073 about?

NCT01633073 is a clinical study titled "A Comparison of the Laryngeal Mask Airway (LMA) Supreme and I-gel in Children". The aim of this randomized prospective study is to compare two single-use laryngeal mask airways with a provision of a gastric drain tube allowing for evacuation of gastric contents, the i-gel and the LMA Supreme, in pediatric patients undergoing positive pressure ventilation. The investigators hypo...

What is the current status of trial NCT01633073?

This trial is currently completed. It is a NA study. The enrollment target is 170 participants. The study started on 2012-06. Estimated completion is 2012-09.

What interventions are being tested in trial NCT01633073?

The interventions under investigation include: LMA Supreme: control device (DEVICE), i-gel: comparison device (DEVICE).

Who is sponsoring clinical trial NCT01633073?

This trial is sponsored by Ann & Robert H Lurie Children's Hospital of Chicago, which has 159 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.