IAPV: Efficacy of Intermittent Abdominal Pressure Ventilation in Neuromuscular Patients

Sponsor
Fondazione Don Carlo Gnocchi Onlus (Other)
Overall Status
Recruiting
CT.gov ID
NCT05346263
Collaborator
(none)
78
1
2
36
2.2

Study Details

Study Description

Brief Summary

Non-Invasive Ventilation (NIV) is an established treatment to manage respiratory muscles dysfunction in neuromuscular disease, preventing the progression of respiratory failure to intubation and/or a tracheotomy. NIV is commonly needed at first during the night, but when the disease worsens, it is required during the day. It is provided via nasal or oronasal masks, causing discomfort and/or aesthetic issues that result in poor compliance.

Intermittent Abdominal Pressure Ventilation (IAPV) is a valid, though unconventional, alternative to daytime NIV: it consists of a portable ventilator with an internal battery and a corset as interface. The IAPV corset is lightweight, comfortable and, thanks to velcro fasteners, easier and better fitting than a face mask. Cyclical inflation of a rubber bladder inside the corset moves the diaphragm upwards like a pneumobelt causing air to enter in the lungs via the upper airways as gravity draws the diaphragm back to its resting position.

IAPV is indicated in neuromuscular disease and has already been tested in few preliminary studies and case reports. This study wants to verify the hypothesis of its application in population of neuromuscular patients.

Condition or Disease Intervention/Treatment Phase
  • Device: Intermittent Abdominal Pressure Ventilation
  • Device: Usual ventilation
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
78 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Efficacy of Intermittent Abdominal Pressure Ventilation in Neuromuscular Patients: Multicentre, Randomised Controlled Trial
Actual Study Start Date :
Mar 1, 2022
Anticipated Primary Completion Date :
Oct 1, 2023
Anticipated Study Completion Date :
Mar 1, 2025

Arms and Interventions

Arm Intervention/Treatment
Experimental: Experimental Group

Patients in experimental group will be adapted to Intermittent Abdominal Pressure Ventilation (IAPV). Abdominal ventilation replaces part of usual ventilation (non invasive ventilation with mouthpiece or nasal-pillow)

Device: Intermittent Abdominal Pressure Ventilation
Patients of experimental group will use IAPV in daytime ventilation. Intermittent abdominal pressure ventilation (IAPV) is a portable ventilator with an internal battery and PneumoBelt corset as an interface.
Other Names:
  • IAPV
  • Active Comparator: Control Group

    Patients in control group continue with usual ventilation (NIV through mouthpiece or nasal-pillow)

    Device: Usual ventilation
    NIV

    Outcome Measures

    Primary Outcome Measures

    1. Changes of respiratory parameters assessed by blood gas analysis [12 months]

      Changes of respiratory parameters in terms of normalization of oxyemia (Arterial Pressure of oxygen 80-100 mmHg) and normalization of capnia (Arterial Pressure of carbon dioxide 35-45 mmHg), assessed by blood gas analysis

    Secondary Outcome Measures

    1. Therapy adherence [12 months]

      Adherence to IAPV tested with Beliefs about Ventilation Questionnaire (BVQ). BVQ is a qualitative questionnaire: it consist of 25 items, where higher scores mean a better outcome.

    2. Patients and caregivers satisfaction to IAPV [12 months]

      Satisfaction to IAPV tested with Visual Analog Scale (VAS), with a score that ranges between 0 and 10, where a higher score means a worse outcome.

    3. Amelioration of Quality of life [12 months]

      Improvement of quality of life tested with World Health Organization Quality of Life-Brief (WHOQOL-Brief), with a score ranging from 0 to 100 for each of the four domain and where a higher score means a better outcome

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Diagnosis of Neuromuscular Disease (Amyotrophic Lateral Sclerosis, Duchenne Muscular Dystrophy, Spinal Muscular Atrophy, Pompe Disease)

    • Non Invasive Ventilation > 16 hours/day

    • Informed consent signed

    Exclusion Criteria:
    • Diagnosis of kyphoscoliosis

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 IRCCS S. Maria Nascente - Fondazione Don Carlo Gnocchi Milan Italy 20146

    Sponsors and Collaborators

    • Fondazione Don Carlo Gnocchi Onlus

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Fondazione Don Carlo Gnocchi Onlus
    ClinicalTrials.gov Identifier:
    NCT05346263
    Other Study ID Numbers:
    • 19/2021/CE_FdG/FC/SA
    First Posted:
    Apr 26, 2022
    Last Update Posted:
    Apr 26, 2022
    Last Verified:
    Mar 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Fondazione Don Carlo Gnocchi Onlus
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 26, 2022