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NCT03080896 · ClinicalTrials.gov registry record · NA

Video-Laryngoscope Alone or With Bronchoscope for Predicted Difficult Intubation

A NA study of Intubation; Difficult, sponsored by University of Louisville.

Completed
Registry status
NA
Development phase
80
Enrollment target
1
Study location

NCT03080896 is a NA study of Intubation; Difficult that has completed, run by University of Louisville. The registered enrollment target is 80 participants. The trial reports 1 study location across 1 state.

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The verdict

NCT03080896, a NA study of Intubation; Difficult, has completed, sponsored by University of Louisville.

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

Study Summary

Using a combination of the video-laryngoscope with the disposable fiber-optic bronchoscope (aScope III) is a feasible way to facilitate successful intubation in a timely manner, in patients with predicted difficult airway due to tumors in the oral cavity, pharynx or larynx To test the hypothesis that combination of video-laryngoscope with the fiber-optic bronchoscope is superior to video-laryngoscope alone for intubation of patients with oral cavity, pharyngeal or laryngeal pathologies undergoing surgery

Conditions Studied

Interventions

  • DEVICE King Vision video-laryngoscope with #3 disposable blade and endotracheal tube stylet
  • DEVICE fiberoptic bronchoscope aScope III

Study Locations (1)

Kentucky

  • University of Louisville Medical School, Department of Anesthesiology and Perioperative Medicine - Louisville

Trial Details

FieldValue
Enrollment Target 80 participants
Start Date 2017-04-10
Est. Completion 2024-03-31
Phase NA

Sponsor

University of Louisville

217 total trials

What the Registry Record Tells You About NCT03080896

The ClinicalTrials.gov registry entry for NCT03080896 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 80 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Louisville, which has 217 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Intubation; Difficult appearing as the primary indexed condition, and to 2 interventions - of which King Vision video-laryngoscope with #3 disposable blade and endotracheal tube stylet is the first listed.

NCT03080896 reports 1 study location spanning 1 distinct geographic area - top geographies include Kentucky.

Frequently Asked Questions

What is clinical trial NCT03080896 about?

NCT03080896 is a clinical study titled "Video-Laryngoscope Alone or With Bronchoscope for Predicted Difficult Intubation". Using a combination of the video-laryngoscope with the disposable fiber-optic bronchoscope (aScope III) is a feasible way to facilitate successful intubation in a timely manner, in patients with predicted difficult airway due to tumors in the oral cavity, pharynx or larynx To test the hypothesis tha...

What is the current status of trial NCT03080896?

This trial is currently completed. It is a NA study. The enrollment target is 80 participants. The study started on 2017-04-10. Estimated completion is 2024-03-31.

What conditions does trial NCT03080896 study?

This clinical trial studies the following conditions: Intubation; Difficult.

What interventions are being tested in trial NCT03080896?

The interventions under investigation include: King Vision video-laryngoscope with #3 disposable blade and endotracheal tube stylet (DEVICE), fiberoptic bronchoscope aScope III (DEVICE).

Who is sponsoring clinical trial NCT03080896?

This trial is sponsored by University of Louisville, which has 217 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03080896 being conducted?

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

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