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NCT01924559 · ClinicalTrials.gov registry record · NA
Comparison of Airway Intubation Devices When Using a Biohazard Suit
A NA study, sponsored by Lehigh Valley Hospital.
- Completed
- Registry status
- NA
- Development phase
- 37
- Enrollment target
NCT01924559 is a NA study that has completed, run by Lehigh Valley Hospital. The registered enrollment target is 37 participants.
The verdict
NCT01924559, a NA study, has completed, sponsored by Lehigh Valley Hospital.
- COMPLETED
- Registry status
- NA
- Development phase
- 37 participants
- Enrollment target
Study Summary
We will investigate the impact biohazard gear has on time to successful intubation and, in particular, determine how the Supraglottic Airway Laryngopharyngeal Tube (Ecolab, Columbus, Missouri) device compares to traditional direct laryngoscopy and fiber-optic (video) intubation techniques.
Interventions
- DEVICE Direct Laryngoscopy
- DEVICE Glidescope
- OTHER standard clothing
- OTHER Biohazard gear
- DEVICE Supraglottic Airway
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 37 participants |
| Start Date | 2013-08 |
| Est. Completion | 2013-09 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01924559
The ClinicalTrials.gov registry entry for NCT01924559 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 37 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Lehigh Valley Hospital, which has 16 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 5 interventions - of which Direct Laryngoscopy is the first listed.
NCT01924559 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01924559 about?
NCT01924559 is a clinical study titled "Comparison of Airway Intubation Devices When Using a Biohazard Suit". We will investigate the impact biohazard gear has on time to successful intubation and, in particular, determine how the Supraglottic Airway Laryngopharyngeal Tube (Ecolab, Columbus, Missouri) device compares to traditional direct laryngoscopy and fiber-optic (video) intubation techniques.
What is the current status of trial NCT01924559?
This trial is currently completed. It is a NA study. The enrollment target is 37 participants. The study started on 2013-08. Estimated completion is 2013-09.
What interventions are being tested in trial NCT01924559?
The interventions under investigation include: Direct Laryngoscopy (DEVICE), Glidescope (DEVICE), standard clothing (OTHER), Biohazard gear (OTHER), Supraglottic Airway (DEVICE).
Who is sponsoring clinical trial NCT01924559?
This trial is sponsored by Lehigh Valley Hospital, which has 16 total clinical trials registered on ClinicalTrials.gov.
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