Actively Recruiting

Phase Not Applicable
Age: 18Years - 90Years
All Genders
Healthy Volunteers
NCT05724745

Evaluation of 3D Magnetic Resonance Spirometry: Comparison with Spirometry in Healthy Subjects and Patients with Respiratory Pathologies (asthma, COPD, Bilateral Lung Transplant)

Led by Commissariat A L'energie Atomique · Updated on 2025-02-14

240

Participants Needed

1

Research Sites

257 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Spirometry is now the gold standard technique for assessing lung function in humans. From the shape of a flow-volume curve measured while the patient, trained by the practitioner, performs forced breaths, the forced vital capacity (FVC) and the forced expiratory volume in one second (FEV1) can be deduced and the pulmonologist is able to detect and characterize respiratory diseases as well as to evaluate current treatments. This technique is non-invasive and simple. It is widely available, robust, reproducible and sensitive to intervention. However, it requires proactive cooperation from the patient and only measures global pulmonary ventilation, without locoregional information. An innovative strategy and an original study framework have been developed in the BioMaps laboratory to establish local maps of flow-volume curves across the lung and to jointly analyze ventilatory function and mechanical behavior at any point in the lung: 3D magnetic resonance spirometry. As respiratory mechanics fundamentally supports ventilatory function, this technique should open a new avenue to non-invasively explore lung function while providing a better diagnosis of regional lung diseases.

CONDITIONS

Official Title

Evaluation of 3D Magnetic Resonance Spirometry: Comparison with Spirometry in Healthy Subjects and Patients with Respiratory Pathologies (asthma, COPD, Bilateral Lung Transplant)

Who Can Participate

Age: 18Years - 90Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Ability to understand the study and give informed consent
  • Ability to remain still in an MRI scanner in supine position for the scan duration
  • Healthy volunteers aged 18-45 years without known lung diseases and non-smokers
  • Asthma patients aged 18-80 years with moderate or severe asthma diagnosed for at least 6 months and non-smokers/non-vapourists
  • COPD patients aged 40-80 years with moderate to severe COPD
  • Bilateral lung transplant patients aged 18-90 years with or without bronchiolitis obliterans syndrome (BOS) meeting specific lung function and imaging criteria
Not Eligible

You will not qualify if you...

  • Presence of visible lung parenchymal opacities on CT scan (mixed RAS/CLAD)
  • Significant bronchial stenosis requiring endoscopic treatment
  • Diaphragmatic impairment confirmed by sniff test or ultrasound
  • Current smokers or vapour users (for asthma and healthy volunteers)
  • Inability to remain motionless during MRI scans

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

CEA | Service Hospitalier Fréderic Joliot

Orsay, France, France, 91401

Actively Recruiting

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Research Team

M

MARTINS Bernadette

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

OTHER

Number of Arms

1

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Evaluation of 3D Magnetic Resonance Spirometry: Comparison with Spirometry in Healthy Subjects and Patients with Respiratory Pathologies (asthma, COPD, Bilateral Lung Transplant) | DecenTrialz