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NCT00706823 · ClinicalTrials.gov registry record · NA
Comparison of I-gel to the Laryngeal Mask Airway
A NA study of Supraglottic Airway and Endotracheal Intubation, sponsored by The University of Texas Health Science Center, Houston.
- Completed
- Registry status
- NA
- Development phase
- 50
- Enrollment target
- 1
- Study location
NCT00706823 is a NA study of Supraglottic Airway and Endotracheal Intubation that has completed, run by The University of Texas Health Science Center, Houston. The registered enrollment target is 50 participants, below the 12,247-participant average among 3 other Supraglottic Airway trials with a reported enrollment target (100% lower). The trial reports 1 study location across 1 state.
The verdict
NCT00706823, a NA study of Supraglottic Airway and Endotracheal Intubation, has completed, sponsored by The University of Texas Health Science Center, Houston.
- COMPLETED
- Registry status
- NA
- Development phase
- 50 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is to evaluate a new disposable supra-glottic airway device, the i-gel airway (Intersurgical Ltd., Wokingham, England). We propose to test its ease of insertion, position within the airway, drain tube patency and anatomic sealing properties during mechanical ventilation in non-obese anesthetized patients undergoing elective general surgery. The study device will be compared to the current standard in the industry, the LMA Unique.
Conditions Studied
Interventions
- DEVICE i-gel airway (Intersurgical Ltd., Wokingham, England)
- DEVICE Laryngeal Mask Airway-Unique
Study Locations (1)
Texas
- Memorial Hermann Hospital - Houston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 50 participants |
| Start Date | 2008-02 |
| Est. Completion | 2008-08 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00706823
The ClinicalTrials.gov registry entry for NCT00706823 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 50 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 12,247-participant average among 3 other Supraglottic Airway trials with a reported enrollment target (100% lower). The listed sponsor is The University of Texas Health Science Center, Houston, which has 732 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Supraglottic Airway appearing as the primary indexed condition, and to 2 interventions - of which i-gel airway (Intersurgical Ltd., Wokingham, England) is the first listed.
NCT00706823 reports 1 study location spanning 1 distinct geographic area - top geographies include Texas.
Frequently Asked Questions
What is clinical trial NCT00706823 about?
NCT00706823 is a clinical study titled "Comparison of I-gel to the Laryngeal Mask Airway". The purpose of this study is to evaluate a new disposable supra-glottic airway device, the i-gel airway (Intersurgical Ltd., Wokingham, England). We propose to test its ease of insertion, position within the airway, drain tube patency and anatomic sealing properties during mechanical ventilation in ...
What is the current status of trial NCT00706823?
This trial is currently completed. It is a NA study. The enrollment target is 50 participants. The study started on 2008-02. Estimated completion is 2008-08.
What conditions does trial NCT00706823 study?
This clinical trial studies the following conditions: Supraglottic Airway, Endotracheal Intubation.
What interventions are being tested in trial NCT00706823?
The interventions under investigation include: i-gel airway (Intersurgical Ltd., Wokingham, England) (DEVICE), Laryngeal Mask Airway-Unique (DEVICE).
Who is sponsoring clinical trial NCT00706823?
This trial is sponsored by The University of Texas Health Science Center, Houston, which has 732 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00706823 being conducted?
This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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