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Physiological Effects of HFNC During Exercise in Patients With Fibrosing Interstitial Lung Diseases (HighFlowMusc)

A

ADIR Association

Status

Enrolling

Conditions

Pulmonary Rehabilitation
Interstitial Lung Disease

Treatments

Device: high flow nasal canulae
Device: Ventury mask

Study type

Interventional

Funder types

Other

Identifiers

NCT05372926
HighFlowMusc

Details and patient eligibility

About

in this study, the investigators aim to describe the effects of highflow nasal canulae oxygen therapy (HFNC) on respiratory muscle function during exercise in patients with fibrosing interstitial lung diseases (ILD) during an endurance test

Enrollment

16 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Cared for as part of a respiratory rehabilitation program (ADIR association)
  • Presenting diffuse fibrosing interstitial pneumonitis, documented by CT scan data and whatever its etiology
  • Presenting severe hypoxemia in ambient air (SpO2<90%) during an exercise test (6-minute walk test or functional exercise test)

Exclusion criteria

  • Patient with a contraindication to carrying out a respiratory rehabilitation program
  • Patient having presented an exacerbation of PID, pneumothorax or pneumomediastinum in the 3 months preceding potential inclusion
  • Tracheostomized patient
  • Patient with a contraindication to the placement of a nasogastric tube
  • Pregnant or breastfeeding women or women of childbearing age without effective means of contraception (a pregnancy test will be carried out)
  • Protected adult patient (guardianship or curatorship)
  • Patient deprived of liberty by court or administrative decision
  • Refusal of patient participation or consent

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

16 participants in 2 patient groups

Venturi mask
Experimental group
Description:
Patients will be placed under oxygen therapy with Venturi mask at a constant flow of 15L/min and a set FiO2 of 50%. The real FiO2 will be mesured in the mask at rest.
Treatment:
Device: Ventury mask
High flow nasal canulae
Experimental group
Description:
Patients will be placed under high flow nasal canulae oxygen therapy with a constant flow of 50L/min and the real FiO2 provided by Venturi mask.
Treatment:
Device: high flow nasal canulae

Trial contacts and locations

1

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Central trial contact

Elise ARTAUD-MACARI, MD; Maryline LEFORT

Data sourced from clinicaltrials.gov

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