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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.

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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

FieldValue
Enrollment Target 37 participants
Start Date 2013-08
Est. Completion 2013-09
Phase NA

Sponsor

Lehigh Valley Hospital

16 total trials

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.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.