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Clinical Trial Summary

This protocol aims to evaluate the feasibility and benefit of Intrapulmonary Percussive Ventilation (IPV) to improve deposition of inhaled radiolabelled aerosols in fibrotic lung regions of patients with Idiopathic Pulmonary Fibrosis (IPF). Phase 1 of the protocol aims to identify the highest IPV pressure that is tolerated by individual patients. Secondary endpoints explore safety of IPV in IPF patients. Phase 2 of the protocol is a crossover randomized trial where patients will inhale 99mTc-labelled DiethyleneTriamine PentaAcetate (DTPA) aerosols with or without IPV. Aerosol deposition in HRCT-defined fibrotic regions of interest (ROI) is described by Single Photon Emission Computed Tomography (SPECT).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05366387
Study type Interventional
Source University Hospital, Tours
Contact Laurent PLANTIER, MD-PhD
Phone 02 47 47 98 44
Email laurent.plantier@univ-tours.fr
Status Recruiting
Phase N/A
Start date November 23, 2022
Completion date May 2024

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