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
About this trial
This is an interventional other trial for Shortness of Breath
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)
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
NCT ID
NCT04332198
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
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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