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Neurobiological and Immunological Mechanisms of Dyspnea in ALS (BIOPNEA)

Primary Purpose

Shortness of Breath, Dyspnea, Amyotrophic Lateral Sclerosis

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
biological test
Sponsored by
Association pour le Développement et l'Organisation de la Recherche en Pneumologie et sur le Sommeil
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Shortness of Breath

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

- Patients with chronic respiratory failure with diaphragmatic dysfunction linked to amyotrophic lateral sclerosis and requiring long-term NIV

Exclusion Criteria:

  • Other respiratory disease (COPD, asthma, obstructive sleep apnea)
  • Alcohol or psychotropic drug the lasts 24 hours
  • Cognitive impairment
  • Smoking > 10 PA
  • Exacerbation or infection 6 weeks earlier
  • Endstage of illness
  • Chronic or acute pain (VAS > 3)

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Experimental

    Arm Label

    ALS patients

    Arm Description

    Outcomes

    Primary Outcome Measures

    the cytokines and endorphins rates variation after initiation of NIV in ALS patients
    measure cytokines and endorphins blood levels before and after NIV

    Secondary Outcome Measures

    Full Information

    First Posted
    March 31, 2020
    Last Updated
    February 17, 2022
    Sponsor
    Association pour le Développement et l'Organisation de la Recherche en Pneumologie et sur le Sommeil
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    1. Study Identification

    Unique Protocol Identification Number
    NCT04332198
    Brief Title
    Neurobiological and Immunological Mechanisms of Dyspnea in ALS (BIOPNEA)
    Official Title
    Neurobiological and Neuro-immunological Mechanisms of Dyspnea in Amyotrophic Lateral Sclerosis
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    February 2022
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    July 2023 (Anticipated)
    Primary Completion Date
    October 2024 (Anticipated)
    Study Completion Date
    October 2024 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Association pour le Développement et l'Organisation de la Recherche en Pneumologie et sur le Sommeil

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No

    5. Study Description

    Brief Summary
    Dyspnea; subjective experience of respiratory discomfort; which produces negative emotional experience, is the most common symptom of patients afflicted with chronic respiratory failure and its treatments are limited. Amyotrophic Lateral Sclerosis (ALS) related - dyspnea, due to diaphragmatic dysfunction, is similar to dyspnea during mechanical inspiratory load (activation of the supplementary motor area, SMA). The perception of pain and dyspnea is processed in similar brain areas (insula, dorsal anterior cingulate cortex, amygdala and medial thalamus) and in ALS; relieving dyspnea by noninvasive ventilation (NIV) is associated with decreased pain thresholds. Otherwise, it is reported systemic elevations of pro-inflammatory cytokines in chronic pain patients, correlating with intensity of pain, and during respiratory load in healthy volunteers. The objectives are to evaluate the cytokines and endorphins rates variations after initiation of NIV in ALS patients, and to correlate cytokines and endorphins rates with the intensity of the affective component and the intensity of the sensory component of dyspnea. The investigators will perform a prospective, experimental study, including 30 ALS patients. Dyspnea, ventilatory and cardiac settings, electromyographic recording of the scalene muscle and biological assays (ACTH, endorphin, Neuropeptide P, BDNF, IL1, IL6, IL8, IL10, TNF), will be measured during spontaneous breathing and during NIV at different times after initiation. The investigators expect a reduction of immunological and neurobiological markers after relieving dyspnea by NIV. This work could lead to the development of new treatments for dyspnea.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Shortness of Breath, Dyspnea, Amyotrophic Lateral Sclerosis

    7. Study Design

    Primary Purpose
    Other
    Study Phase
    Not Applicable
    Interventional Study Model
    Single Group Assignment
    Masking
    None (Open Label)
    Allocation
    N/A
    Enrollment
    30 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    ALS patients
    Arm Type
    Experimental
    Intervention Type
    Other
    Intervention Name(s)
    biological test
    Other Intervention Name(s)
    questionnaire
    Intervention Description
    dyspnea evaluation, ventilatory evaluation and biological test before and after non invasive ventilation
    Primary Outcome Measure Information:
    Title
    the cytokines and endorphins rates variation after initiation of NIV in ALS patients
    Description
    measure cytokines and endorphins blood levels before and after NIV
    Time Frame
    30 minutes

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: - Patients with chronic respiratory failure with diaphragmatic dysfunction linked to amyotrophic lateral sclerosis and requiring long-term NIV Exclusion Criteria: Other respiratory disease (COPD, asthma, obstructive sleep apnea) Alcohol or psychotropic drug the lasts 24 hours Cognitive impairment Smoking > 10 PA Exacerbation or infection 6 weeks earlier Endstage of illness Chronic or acute pain (VAS > 3)

    12. IPD Sharing Statement

    Learn more about this trial

    Neurobiological and Immunological Mechanisms of Dyspnea in ALS (BIOPNEA)

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