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Mask Leak With Nasal Cannula in Noninvasive Positive Pressure Ventilation

NCT02743936 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 64

Last updated 2016-09-26

Study results available
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Summary

This is a prospective randomized cross over study of healthy volunteers undergoing continuous positive airway pressure ventilation via a noninvasive ventilation (NIV) mask with and without the addition of nasal cannulas. Mask leak will be measured by the ventilator after 60 seconds of spontaneous resting ventilation, with each subject serving as his or her own control.

Conditions

  • Mechanical Ventilation Pressure High

Interventions

DEVICE

Nasal cannula

Placement of nasal cannula under non-invasive positive pressure ventilation mask

DEVICE

Non-invasive positive pressure ventilation

Non-invasive positive pressure ventilation

Sponsors & Collaborators

  • Brooke Army Medical Center

    lead FED

Principal Investigators

  • Michael D April, MD, PhD, MSc · Brooke Army Medical Center

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2016-04-30
Primary Completion
2016-05-31
Completion
2016-05-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02743936 on ClinicalTrials.gov