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NCT00581386 · ClinicalTrials.gov registry record · NA
Clinical Comparison of the Airway Devices
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
- 218
- Enrollment target
- 1
- Study location
NCT00581386: Completed NA study of Supraglottic Airway and Endotracheal Intubation, sponsored by The University of Texas Health Science Center, Houston.
NCT00581386 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 218 participants, below the 12,191-participant average among 3 other Supraglottic Airway trials with a reported enrollment target (98% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00581386, 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
- 218 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is to evaluate a new supra-glottic airway device, the "Disposable Laryngeal Tube Suction" (LTS-D; King Systems, Noblesville, IN). We propose to test its ease of insertion, position within the airway, patency of drain tube and anatomic sealing properties during spontaneous ventilation in anesthetized patients. The study device will be compared to the ProSeal Laryngeal Mask Airway (PLMA, LMA North America Inc.) and the Esophageal Tracheal Combitube (ETC; Tyco Healthcare/Mallinckrodt Nellcor, Pleasanton, Calif).
Primary Outcome
The time taken to successfully place the device in seconds.
Conditions Studied
Interventions
- DEVICE LTS-D
- DEVICE ProSeal Laryngeal Mask Airway
- DEVICE Esophageal Tracheal Combitube (ETC)
Study Locations (1)
Texas
- Memorial Hermann Hospital - Houston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 218 participants |
| Start Date | 2007-05 |
| Est. Completion | 2009-04 |
| Phase | NA |
What the finished NCT00581386 record still lists
NCT00581386 is an interventional study that assigns participants to a tested intervention. The registered 218 participants enrollment target is mid-sized for trials with a published cap, below the 12,191-participant average among 3 other Supraglottic Airway trials with a reported enrollment target (98% lower).
The record links to 2 conditions, with Supraglottic Airway appearing as the primary indexed condition, and to 3 interventions - of which LTS-D is the first listed.
NCT00581386 reports a single indexed study location in Texas.
Frequently Asked Questions
What is clinical trial NCT00581386 about?
NCT00581386 is a clinical study titled "Clinical Comparison of the Airway Devices". The purpose of this study is to evaluate a new supra-glottic airway device, the "Disposable Laryngeal Tube Suction" (LTS-D; King Systems, Noblesville, IN). We propose to test its ease of insertion, position within the airway, patency of drain tube and anatomic sealing properties during spontaneous v...
What is the current status of trial NCT00581386?
This trial is currently completed. It is a NA study. The enrollment target is 218 participants. The study started on 2007-05. Estimated completion is 2009-04.
What conditions does trial NCT00581386 study?
This clinical trial studies the following conditions: Supraglottic Airway, Endotracheal Intubation.
What interventions are being tested in trial NCT00581386?
The interventions under investigation include: LTS-D (DEVICE), ProSeal Laryngeal Mask Airway (DEVICE), Esophageal Tracheal Combitube (ETC) (DEVICE).
Who is sponsoring clinical trial NCT00581386?
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 NCT00581386 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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