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NCT01683526 · ClinicalTrials.gov registry record · NA

Safety and Efficacy of Endotracheal Intubation Using Glidescope Video-Laryngoscope

A NA study of Respiratory Failure, sponsored by Beth Israel Medical Center.

Completed
Registry status
NA
Development phase
117
Enrollment target
1
Study location

NCT01683526 is a NA study of Respiratory Failure that has completed, run by Beth Israel Medical Center. The registered enrollment target is 117 participants, below the 4,521-participant average among 40 other Respiratory Failure trials with a reported enrollment target (97% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT01683526, a NA study of Respiratory Failure, has completed, sponsored by Beth Israel Medical Center.

COMPLETED
Registry status
NA
Development phase
117 participants
Enrollment target
1
Study location

Study Summary

The safety and efficacy of a video-laryngoscope as a primary intubation tool in urgent endotracheal intubation of critically-ill patients has not been well-described in the literature. This study will answer whether using a VL will impact on the efficacy and safety of intubation compared with a traditional direct laryngoscopy.

Conditions Studied

Interventions

  • PROCEDURE Direct laryngoscopy
  • DEVICE Video laryngoscopy (Glidescope)

Study Locations (1)

New York

  • Beth Isreal Medical Center - New York

Trial Details

FieldValue
Enrollment Target 117 participants
Start Date 2012-08
Est. Completion 2013-04
Phase NA

Sponsor

Beth Israel Medical Center

44 total trials

What the Registry Record Tells You About NCT01683526

The ClinicalTrials.gov registry entry for NCT01683526 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 117 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 4,521-participant average among 40 other Respiratory Failure trials with a reported enrollment target (97% lower). The listed sponsor is Beth Israel Medical Center, which has 44 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Respiratory Failure appearing as the primary indexed condition, and to 2 interventions - of which Direct laryngoscopy is the first listed.

NCT01683526 reports 1 study location spanning 1 distinct geographic area - top geographies include New York.

Frequently Asked Questions

What is clinical trial NCT01683526 about?

NCT01683526 is a clinical study titled "Safety and Efficacy of Endotracheal Intubation Using Glidescope Video-Laryngoscope". The safety and efficacy of a video-laryngoscope as a primary intubation tool in urgent endotracheal intubation of critically-ill patients has not been well-described in the literature. This study will answer whether using a VL will impact on the efficacy and safety of intubation compared with a trad...

What is the current status of trial NCT01683526?

This trial is currently completed. It is a NA study. The enrollment target is 117 participants. The study started on 2012-08. Estimated completion is 2013-04.

What conditions does trial NCT01683526 study?

This clinical trial studies the following conditions: Respiratory Failure.

What interventions are being tested in trial NCT01683526?

The interventions under investigation include: Direct laryngoscopy (PROCEDURE), Video laryngoscopy (Glidescope) (DEVICE).

Who is sponsoring clinical trial NCT01683526?

This trial is sponsored by Beth Israel Medical Center, which has 44 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01683526 being conducted?

This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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

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