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Long-Term Effect of LIAM on Respiratory Performance in NIV Patients Suffering From Neuromuscular Disease

C

Centre d'Investigation Clinique et Technologique 805

Status

Unknown

Conditions

Neuromuscular Disease

Treatments

Device: non invasive mechanical ventilation

Study type

Interventional

Funder types

Other

Identifiers

NCT02288299
2014-A01005-42

Details and patient eligibility

About

The long-term effect of LIAM (Lung Insufflation Assist Maneuver) on respiratory performance in home non-invasively ventilated (NIV) patients suffering from neuromuscular disease will be assessed in a prospective, randomized, cross over, open label study

Full description

In advanced neuromuscular disorders, respiratory complications represent the main cause of morbidity and mortality. Beside chronic respiratory insufficiency, necessitating a ventilatory support, mostly performed by non-invasive ventilation (NIV), cough is impaired due to the muscle weakness, and respiratory physiotherapy becomes an essential part of the management.

Various techniques have been proposed to improve lung recruitment and cough in neuromuscular patients. The assisted techniques based on a positive pressure insufflation maneuver have shown an improvement in physiological variables on the short term, but there is to date no good-quality prospective study allowing to evaluate the long term efficacy of mechanical cough assistance devices in neuromuscular patients.

We designed a randomized, cross over, open label study to assess the long-term effect of LIAM (Lung Insufflation Assist Maneuver) on respiratory performance in NIV patients suffering from neuromuscular disease.

Enrollment

30 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • o neuromuscular disease ( progressive muscular dystrophy, for example; Duchenne muscular dystrophy, spinal muscular atrophy)

    • age ≥ 18 years
    • indication to NIV (ongoing ventilation or new patients)
    • vital capacity ≤ 50% pred
    • peak cough flow < 270 l/min
    • "LIAM Responder" = increased insufflation capacity (≥ + 50%) and Peak Cough Flow (PCF ≥+ 50%) with LIAM

Exclusion criteria

  • o acute respiratory failure (respiratory acidosis)

    • home treatment by instrumental cough assistance in the preceding 12 months
    • ongoing medical treatment of the neuromuscular disease (for ex: corticosteroids in Duchenne disease, enzyme therapy in Pompe disease)
    • previous pneumothorax
    • plan of legal protection
    • pregnant or breastfeeding women
    • failure to cooperate
    • no affiliation to a social security scheme

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

30 participants in 1 patient group

non invasive mechanical ventilation
Experimental group
Description:
Patients suffering from neuromuscular disease with NIV indication and cough inefficiency
Treatment:
Device: non invasive mechanical ventilation

Trial contacts and locations

1

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Central trial contact

Frederic Lofaso, MD, PhD; David Orlikowski, MD, PhD

Data sourced from clinicaltrials.gov

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