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COMPLETED NA

Video-Laryngoscope Alone or With Bronchoscope for Predicted Difficult Intubation

NCT03080896 · View on ClinicalTrials.gov ↗

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

260 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT03080896

The ClinicalTrials.gov registry entry for NCT03080896 describes a study currently listed as completed. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. 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 260 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

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. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT03080896 reports 1 study location spanning 1 distinct geographic area — top geographies include Kentucky. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

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. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

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). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT03080896?

This trial is sponsored by University of Louisville, which has 260 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

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.

Related

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