Actively Recruiting

Phase Not Applicable
Age: 18Years - 100Years
All Genders
NCT06249412

The Importance of Positive Expiratory Pressure Associated With the In-exsufflator in ALS Patients

Led by Groupe Hospitalier du Havre · Updated on 2026-01-21

11

Participants Needed

1

Research Sites

114 weeks

Total Duration

On this page

Sponsors

G

Groupe Hospitalier du Havre

Lead Sponsor

F

French Physiotherapy Society / Société Français de Physiothérapie

Collaborating Sponsor

AI-Summary

What this Trial Is About

Amyotrophic Lateral Sclerosis (ALS) is a fatal neurodegenerative disorder that impairs motor neurons, with a life expectancy of 2 to 7 years after diagnosis. ALS manifests as 'spinal' when it primarily affects limbs, or 'bulbar' when it impairs speech and swallowing. The disease progressively weakens all skeletal muscles, causing respiratory issues and increased risk of lung infections due to ineffective coughing. Mechanical cough assistance via In-exsufflation therapy/ mechanical in-exsufflator devie (INEX/MI-E) applies positive and negative airway pressures non-invasively to improve coughing. However, MI-E may fail in some ALS patients due to airway collapse, often related to brainstem muscle dysfunction.Research by Andersen et al. in 2017 highlighted that during MI-E, ALS patients often experience adverse laryngeal movements, which can obstruct airways and reduce the therapy's effectiveness. To combat this, they suggested individualized MI-E settings to minimize airway collapse. Modern MI-E devices, such as the EOVE-70, offer adjustable positive expiratory pressure (PEP) between cycles to potentially enhance airway stability and coughing efficiency. The current study focuses on the impact of PEP during therapy pauses on the peak expiratory flow rate in ALS patients, which could lead to improved therapeutic outcomes.

CONDITIONS

Official Title

The Importance of Positive Expiratory Pressure Associated With the In-exsufflator in ALS Patients

Who Can Participate

Age: 18Years - 100Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Male or female patient aged over 18 years
  • Patient diagnosed with Amyotrophic Lateral Sclerosis (ALS)
  • Patients with established or beginning bulbar symptoms such as speech impairment, hypersalivation, or swallowing difficulties
  • Patient naive to In-exsufflation (INEX) therapy but prescribed for installation or patient already treated with an INEX device
  • Patient followed by the ALS mobile team of the Groupe Hospitalier du Havre or the CHU of Dijon
  • Disease progression compatible with inclusion as judged by medical team
  • Patient willing to participate after receiving adequate information
  • Patient covered by social security or a similar scheme
Not Eligible

You will not qualify if you...

  • Recent respiratory infection episode within the past month
  • Mental illness interfering with proper use of the device
  • History of laryngospasm
  • Inability to attend consultations with the ALS team at the Groupe Hospitalier du Havre or CHU of Dijon
  • Pregnancy
  • Person deprived of liberty by judicial or administrative decision or under legal protection measures
  • Presence of any non-inclusion criterion
  • Refusal to participate after inclusion
  • Death from any cause

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 1 location

1

GH Havre

Le Havre, Normandy, France, 76290

Actively Recruiting

Loading map...

Research Team

Y

Yann Combret, PT, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

TREATMENT

Number of Arms

2

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here