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NCT02018146 · ClinicalTrials.gov registry record · NA

Cohort 2 Efficacy of Nasopharyngeal Ventilation With Endotracheal Tube for Surgery

A NA study, sponsored by University of Louisville.

Completed
Registry status
NA
Development phase
41
Enrollment target

NCT02018146 is a NA study that has completed, run by University of Louisville. The registered enrollment target is 41 participants.

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The verdict

NCT02018146, a NA study, has completed, sponsored by University of Louisville.

COMPLETED
Registry status
NA
Development phase
41 participants
Enrollment target

Study Summary

Failed mask ventilation poses an increased risk of de-oxygenation to the patient undergoing general anesthesia. Nasopharyngeal ventilation may be a valid alternative for mask ventilation allowing for better oxygenation during the induction phase of general anesthesia. Oxygenation may be maintained better in case of difficult mask ventilation. This study evaluates this alternative method in comparison with the standard method of mask ventilation. General Design This is a randomized, controlled, cross over study. Patients will be randomized to mask ventilation followed by nasopharyngeal airway placement and ventilation or vice versa. Primary Study Endpoints We will test the hypothesis that ventilation via a nasally placed ETT is superior in its efficacy (as measured by tidal volume) to routine facemask ventilation in patients undergoing general anesthesia and endotracheal intubation for their surgery.

Interventions

  • OTHER Mask then nasopharyngeal
  • OTHER Nasopharyngeal then mask

Trial Details

FieldValue
Enrollment Target 41 participants
Start Date 2015-06
Est. Completion 2018-05
Phase NA

Sponsor

University of Louisville

217 total trials

What the Registry Record Tells You About NCT02018146

The ClinicalTrials.gov registry entry for NCT02018146 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 41 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 0 conditions, and to 2 interventions - of which Mask then nasopharyngeal is the first listed.

NCT02018146 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT02018146 about?

NCT02018146 is a clinical study titled "Cohort 2 Efficacy of Nasopharyngeal Ventilation With Endotracheal Tube for Surgery". Failed mask ventilation poses an increased risk of de-oxygenation to the patient undergoing general anesthesia. Nasopharyngeal ventilation may be a valid alternative for mask ventilation allowing for better oxygenation during the induction phase of general anesthesia. Oxygenation may be maintained b...

What is the current status of trial NCT02018146?

This trial is currently completed. It is a NA study. The enrollment target is 41 participants. The study started on 2015-06. Estimated completion is 2018-05.

What interventions are being tested in trial NCT02018146?

The interventions under investigation include: Mask then nasopharyngeal (OTHER), Nasopharyngeal then mask (OTHER).

Who is sponsoring clinical trial NCT02018146?

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

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

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.