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Dynamic Hyperinflation During Maximal Voluntary Ventilation in Healthy Subjects

C

Centre Hospitalier Universitaire Saint Pierre

Status

Unknown

Conditions

Dynamic Hyperinflation

Treatments

Behavioral: Healthy Subjects

Study type

Interventional

Funder types

Other

Identifiers

NCT02831465
B076201318918

Details and patient eligibility

About

Maximal Voluntary Ventilation (MVV) correlates well with maximal exercise capacity and is used to assess the ventilatory function during exercise in COPD (Chronic Obstructive Pulmonary Disease) patients. Dynamic hyperinflation (DH) often occurs during MVV in COPD and is believed to be due to expiratory flow limitation.

The present study is intended to assess whether DH can also occur during MVV in normal subjects without expiratory flow limitation.

Full description

Maximal voluntary ventilation (MVV) correlates well with maximal exercise capacity and is used to assess the ventilatory function during exercise in COPD (Chronic Obstructive Pulmonary Disease) patients. Dynamic hyperinflation (DH) often occurs during MVV in COPD and is believed to be due to expiratory flow limitation. The present study is intended to assess whether DH can also occur during MVV in normal subjects without expiratory flow limitation.

Study design: healthy subjects with normal lung function will perform MVV at increasing breathing frequencies and maximal tidal volume, from 10 to 100 cycles per minute. Inspiratory capacity (IC) will be measured at rest and after each 12 seconds of MVV in order to detect DH. From the moment DH appeares at a given frequency, only one additional MVV at a higher breathing frequency will be conducted to confirm DH.

Enrollment

45 estimated patients

Sex

All

Ages

40 to 69 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Healthy subjects

Exclusion criteria

  • History of asthma, obstructive syndrome on basic lung function

Trial design

Primary purpose

Basic Science

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

45 participants in 1 patient group

healthy subjects
Experimental group
Description:
Subjects with normal lung function between 40 and 70 years old.
Treatment:
Behavioral: Healthy Subjects

Trial contacts and locations

1

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Central trial contact

Audrey Herpeux; Inge Muylle, MD

Data sourced from clinicaltrials.gov

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