Actively Recruiting
A Pilot Study of a New Ultrasonographic Tool to Assess Regional Pulmonary Strain in Mechanically Ventilated Patients Suffering From Pulmonary Diseases in an Intensive Care Setting
Led by Centre hospitalier de l'Université de Montréal (CHUM) · Updated on 2025-09-18
10
Participants Needed
1
Research Sites
4 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This research aims to develop a new ultrasonographic method to measure regional pulmonary strain in patients who have lung diseases and are receiving mechanical ventilation in an intensive care unit. Mechanical ventilation, while often necessary, can sometimes cause lung injury due to excessive strain or overdistension, especially in patients with severe lung conditions. The study intends to collect initial data on local pleural strain to assist in planning larger studies and potentially help prevent ventilator-induced lung injury. The study involves using lung ultrasonography to image the pleura at four specific locations on the chest in mechanically ventilated patients. The imaging will be performed using a Terason device with a 12L5 linear ultrasound probe, positioned perpendicularly to the pleura. Three consecutive breathing cycles will be recorded at each site. An experienced ultrasonographer and a technician will analyze the images using an algorithm to calculate various pulmonary strain measurements. Participants will undergo lung ultrasound imaging during their ICU stay, with images taken at four predetermined sites on the chest. Researchers will measure several strain components such as lateral and axial deformation and shear using specialized software. The primary outcome is the average absolute lateral deformation measured on the first day. Other measurements include various deformation ranges and shear values. The study's total duration for each participant is based on data collected during Day 1 of their ICU ventilation period.
CONDITIONS
Brief Title
A New Ultrasonographic Tool to Assess Pulmonary Strain in the ICU
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adult intensive care patients under mechanical ventilation
- Diagnosed with pulmonary disease
- Static lung compliance less than 40 mL/cm H2O
You will not qualify if you...
- Obesity with body mass index over 30 kg/m2
- Previous thoracic procedures such as chest tube, thoracotomy, or thoracoscopy
- Intra-abdominal pressure less than 15 mm Hg if known
- Prior participation in this study
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 1 day
Participants undergo lung ultrasonography imaging at 4 predetermined pulmonary areas to assess regional pulmonary strain.
1 visit (in intensive care unit)
Duration - Up to 1 day
Participants are observed during their intensive care stay with assessments of pulmonary strain to help plan future studies.
Assessments occur during ICU stay
Trial Site Locations
Total: 1 location
1
Centre Hospitalier de l'Université de Montréal (CHUM)
Montreal, Quebec, Canada, H2X 3E4
Actively Recruiting
Research Team
M
Martin Girard, MD,FRCPC
J
Julie Desroches, PhD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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