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Clinical Trials/NCT06182956
NCT06182956
Not yet recruiting
Not Applicable

Evaluation of Physiological Effects of Noninvasive Mechanical Ventilation and High-flow Oxygen Therapy for Acute Exacerbations of Interstitial Lung Diseases

ADIR Association1 site in 1 country18 target enrollmentJanuary 1, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Interstitial Lung Disease
Sponsor
ADIR Association
Enrollment
18
Locations
1
Primary Endpoint
Pulmonary compliance
Status
Not yet recruiting
Last Updated
2 years ago

Overview

Brief Summary

The objectives of this study are to compare the physiological consequences of high-flow oxygen therapy and noninvasive mechanical ventilation on ventilation, respiratory work and hemodynamics during acute respiratory failure in diffuse interstitial pneumonia.

Registry
clinicaltrials.gov
Start Date
January 1, 2024
End Date
December 31, 2026
Last Updated
2 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Sponsor
ADIR Association
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Pulmonary compliance

Time Frame: During the intervention, after an exposure of 30 minutes to the oxygen therapy device

Comparison of global pulmonary compliance (Cglob) under noninvasive ventilation (NIV) and high-flow oxygen therapy (HFO) during acute respiratory failure in diffuse interstitial pneumonia.

Secondary Outcomes

  • transpulmonary pressure(During the intervention, after an exposure of 30 minutes to the oxygen therapy device)
  • end-expiratory lung volume(During the intervention, after an exposure of 30 minutes to the oxygen therapy device)
  • respiratory rate(During the intervention, after an exposure of 30 minutes to the oxygen therapy device)
  • inspiratory time(During the intervention, after an exposure of 30 minutes to the oxygen therapy device)
  • ultrasound diaphragmatic strain.(During the intervention, after an exposure of 30 minutes to the oxygen therapy device)
  • diaphragmatic thickening fraction(During the intervention, after an exposure of 30 minutes to the oxygen therapy device)
  • Pulmonary compliance(During the intervention, after an exposure of 30 minutes to the oxygen therapy device)
  • oesophagal pressure swings(During the intervention, after an exposure of 30 minutes to the oxygen therapy device)
  • Tidal volume(During the intervention, after an exposure of 30 minutes to the oxygen therapy device)
  • oesophagal pressure time products(During the intervention, after an exposure of 30 minutes to the oxygen therapy device)
  • cardiac output(During the intervention, after an exposure of 30 minutes to the oxygen therapy device)
  • heart rate(During the intervention, after an exposure of 30 minutes to the oxygen therapy device)
  • driving pressure(During the intervention, after an exposure of 30 minutes to the oxygen therapy device)
  • Global inhomogeneity index(During the intervention, after an exposure of 30 minutes to the oxygen therapy device)
  • Systolic arterial pressures(During the intervention, after an exposure of 30 minutes to the oxygen therapy device)
  • systolic pulmonary arterial pressure(During the intervention, after an exposure of 30 minutes to the oxygen therapy device)
  • tricuspid annular plane systolic excursion(During the intervention, after an exposure of 30 minutes to the oxygen therapy device)
  • transdiaphragmatic pressure variations(During the intervention, after an exposure of 30 minutes to the oxygen therapy device)
  • peak inspiratory flow(During the intervention, after an exposure of 30 minutes to the oxygen therapy device)
  • Diastolic arterial pressures(During the intervention, after an exposure of 30 minutes to the oxygen therapy device)
  • Mean arterial pressure(During the intervention, after an exposure of 30 minutes to the oxygen therapy device)
  • Pulsed oxymetry(During the intervention, after an exposure of 30 minutes to the oxygen therapy device)
  • Dyspnea(During the intervention, after an exposure of 30 minutes to the oxygen therapy device)
  • Comparison of Comfort(During the intervention, after an exposure of 30 minutes to the oxygen therapy device)
  • transdiaphragmatic pressure time products(During the intervention, after an exposure of 30 minutes to the oxygen therapy device)
  • peak expiratory flow(During the intervention, after an exposure of 30 minutes to the oxygen therapy device)
  • left ventricular ejection fraction(During the intervention, after an exposure of 30 minutes to the oxygen therapy device)
  • E/E' ratio(During the intervention, after an exposure of 30 minutes to the oxygen therapy device)
  • right auricular pressure(During the intervention, after an exposure of 30 minutes to the oxygen therapy device)
  • transcutaneous carbon dioxide pressure(During the intervention, after an exposure of 30 minutes to the oxygen therapy device)
  • right ventricular strain(During the intervention, after an exposure of 30 minutes to the oxygen therapy device)

Study Sites (1)

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