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NCT01449656 · ClinicalTrials.gov registry record
A Comparison of the Laryngeal Mask Airway (LMA) Proseal and LMA Supreme in Children
A clinical trial, sponsored by Ann & Robert H Lurie Children's Hospital of Chicago.
- Completed
- Registry status
- 60
- Enrollment target
NCT01449656 is a clinical trial that has completed, run by Ann & Robert H Lurie Children's Hospital of Chicago. The registered enrollment target is 60 participants.
The verdict
NCT01449656 has completed, sponsored by Ann & Robert H Lurie Children's Hospital of Chicago.
- COMPLETED
- Registry status
- 60 participants
- Enrollment target
Study Summary
The aim of this randomized prospective study is to compare two laryngeal mask airways with a provision for evacuation of gastric contents, the LMA Proseal and The investigators hypothesize that airway leak pressures with the LMA Proseal will be significantly different (higher) when compared with the LMA Supreme.
Interventions
- DEVICE LMA Supreme: comparison device
- DEVICE LMA Proseal: control device
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 60 participants |
| Start Date | 2011-10 |
| Est. Completion | 2011-11 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01449656
The ClinicalTrials.gov registry entry for NCT01449656 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 60 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: comparison device is the first listed.
NCT01449656 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01449656 about?
NCT01449656 is a clinical study titled "A Comparison of the Laryngeal Mask Airway (LMA) Proseal and LMA Supreme in Children". The aim of this randomized prospective study is to compare two laryngeal mask airways with a provision for evacuation of gastric contents, the LMA Proseal and The investigators hypothesize that airway leak pressures with the LMA Proseal will be significantly different (higher) when compared with the...
What is the current status of trial NCT01449656?
This trial is currently completed. The enrollment target is 60 participants. The study started on 2011-10. Estimated completion is 2011-11.
What interventions are being tested in trial NCT01449656?
The interventions under investigation include: LMA Supreme: comparison device (DEVICE), LMA Proseal: control device (DEVICE).
Who is sponsoring clinical trial NCT01449656?
This trial is sponsored by Ann & Robert H Lurie Children's Hospital of Chicago, which has 159 total clinical trials registered on ClinicalTrials.gov.
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