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Shear Wave Elastography of Intercostal Muscles for the Non-invasive Assessment of the Work of BreathinG (SWING)

G

Groupe Hospitalier du Havre

Status

Begins enrollment this month

Conditions

Healthy Adult
COPD

Treatments

Diagnostic Test: Intercostal muscle shear wave elastography (SWE) during standardized inspiratory loading

Study type

Observational

Funder types

Other

Identifiers

NCT07371754
2025-A01528-41

Details and patient eligibility

About

Quantifying respiratory effort is a key step in physiological and clinical research on exercise tolerance, mechanisms of fatigability, and ventilatory impairment. To date, reliable assessment relies on an invasive method: esophageal pressure (Pes) measurement using a balloon catheter inserted into the esophagus. Although Pes provides an indirect estimate of pleural and intrathoracic pressure, it is uncomfortable for patients, requires dedicated equipment, and may limit study participation.

In critically ill patients, a noninvasive approach to quantify respiratory effort would have major clinical and scientific value. In acute respiratory distress, accurately tracking the intensity and evolution of respiratory effort could support earlier therapeutic decision-making.

Shear Wave Elastography (SWE) is an ultrasound technology enabling very high acquisition rates and estimating tissue stiffness from shear-wave propagation induced by an acoustic impulse. Because muscle stiffness is strongly related to force produced during contraction, we hypothesize that intercostal muscle stiffness measured by SWE correlates with respiratory work and increases with rising inspiratory load.

Enrollment

20 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Adult patient with chronic obstructive pulmonary disease (COPD), stage 3-4.

Healthy adult volunteer.

Exclusion criteria

Refusal to participate or withdrawal of consent.

Age < 18 years.

BMI > 35 kg/m².

Pregnancy or breastfeeding.

Inability to understand instructions or cooperate (cognitive impairment, language barrier).

Neurological condition affecting breathing (e.g., recent stroke, ALS, myopathy).

Thoracic condition limiting access to the intercostal muscles (e.g., major chest wall deformity, surgical scar).

Recent thoracic or abdominal surgery (< 3 months).

Known esophageal disease (stricture, achalasia, severe esophagitis, diverticulum, history of perforation).

ENT or tracheal abnormality preventing probe insertion (e.g., tumor, malformation, tracheostomy).

Swallowing disorders or risk of aspiration.

Recent exacerbation (< 6 weeks).

Oxygen therapy > 2 L/min during exertion.

Hemodynamic instability.

Not affiliated with a social security scheme.

Legally protected persons (as defined by law).

Trial design

20 participants in 2 patient groups

Healthy adults
Description:
Participant without respiratory, muscle or thoracic abnormalities
Treatment:
Diagnostic Test: Intercostal muscle shear wave elastography (SWE) during standardized inspiratory loading
COPD group
Description:
Patients with COPD
Treatment:
Diagnostic Test: Intercostal muscle shear wave elastography (SWE) during standardized inspiratory loading

Trial contacts and locations

0

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Central trial contact

Clément Medrinal; Angélique Picard

Data sourced from clinicaltrials.gov

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