Skip to main content
Clinical Trials/NCT05415605
NCT05415605
Completed
Not Applicable

Ultrasound Evaluation of Alveolar Stress by Measurement of Ultrasound Pleural Strain in Healthy Subjects

Centre Hospitalier Universitaire de Nīmes1 site in 1 country30 target enrollmentJuly 24, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Ultrasound Strain Measurement
Sponsor
Centre Hospitalier Universitaire de Nīmes
Enrollment
30
Locations
1
Primary Endpoint
Lung Strain values
Status
Completed
Last Updated
4 months ago

Overview

Brief Summary

In the critical patient, lung ultrasound is routinely performed for acute respiratory distress, adult respiratory distress syndrome and for hemodynamic evaluation. Its diagnostic performance is superior to that of chest radiography in the context of pleuropulmonary parenchymal pathologies. The search for lung sliding is performed to diagnose a pneumothorax or to search for the correct placement of the endotracheal intubation tube. However, this analysis is qualitative and is sometimes difficult to interpret. At present, there is no global evaluation technique at the patient's bed allowing to analyze simultaneously the alveolar recruitment, the pulmonary over-distension and the quality of the lung sliding, whereas the pulmonary damage is most often heterogeneous. The justification of our research project is based on the need to develop and validate a means of global and regional quantification of the mechanical and aeration properties of the lung parenchyma by the analysis of the acoustic markers of the pleura (pleural strain) by the ultrasound technique of speckle tracking. The aim is to establish the normal values of the pleural strain in healthy volunteers, in spontaneous ventilation and then in non-invasive mechanical ventilation, in order to vary the lung volume.

Registry
clinicaltrials.gov
Start Date
July 24, 2022
End Date
July 27, 2022
Last Updated
4 months ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Centre Hospitalier Universitaire de Nīmes
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Healthy volunteer male or female between 18 and 50 years old

Exclusion Criteria

  • History of traumatic or spontaneous pneumothorax
  • History of connective tissue disease
  • Any history of chronic respiratory disease
  • Presence of an ongoing clinical respiratory Ear-Nose-Throat (ENT) or pulmonary syndrome (rhinitis, sinusitis, bronchitis, lung disease)
  • History of gastro-duodenal reflux or stomach surgery

Outcomes

Primary Outcomes

Lung Strain values

Time Frame: during the procedure (30 minutes)

Lung strain values (%) in spontaneous ventilation and then under non-invasive mechanical ventilation (NIV) by varying tidal volume and PEEP

Secondary Outcomes

  • Variations of the strain under NIV in the different pulmonary zones tested(during the procedure (30 minutes))
  • Variations of the strain under NIV in the right ventricle(during the procedure (30 min))
  • Variations of the strain under NIV of the diaphragm(during the procedure (30 minutes))
  • Ultrasound semiology and normal values(during the procedure (30 minutes))
  • Longitudinal and transversal values of lung strain in the different pulmonary zones tested(during the procedure (30 minutes))

Study Sites (1)

Loading locations...

Similar Trials