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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: Completed NA study, sponsored by Ann & Robert H Lurie Children's Hospital of Chicago.
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, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (88% lower). According to ClinicalTrials.gov, the official US trial registry.
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.
Primary Outcome
Airway leak pressures will be measured by recording the circuit pressure at which equilibrium is reached when fresh gas flow is delivered at 3L/min when the pressure limiting valve is closed.
Interventions
- DEVICE LMA Supreme: control device
- DEVICE i-gel: comparison device
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 170 participants |
| Start Date | 2012-06 |
| Est. Completion | 2012-09 |
| Phase | NA |
What the finished NCT01633073 record still lists
NCT01633073 is an interventional study that assigns participants to a tested intervention. The registered 170 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (88% lower).
The record links to 0 conditions, and to 2 interventions - of which LMA Supreme: control device is the first listed.
NCT01633073 does not publish any study locations in the registry export this page uses.
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.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01633073's enrollment target sits among peer trials
170 614th of 2000 higher than 1,382 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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