About this trial
The primary objective of the study is to evaluate the feasibility, the quality and the utility of a polygraphic control at home in order to appreciate the efficacy of the night time non-invasive ventilation (allowing to optimize the ventilator settings when the results are not satisfactory).
Eligibility criteria
Qualifiers
Patient ≥ 18 years;
Patient with chronic respiratory insufficiency has just been posed non-invasive ventilation (NIV) in the hospital, according to the latest international recommendations ;
Affiliation to the social security scheme;
Patient has signed the informed consent form to participate to the study.
Disqualifiers
Patient refusal;
Patient under guardianship;
Patient under AME scheme;
Patients living more than 40 km from reference center;
Trial design
Treatments tested in this trial
- Polygraphy diagnostic at home
Treatment groups
Sponsors and collaborators
Assistance Publique - Hôpitaux de Paris
Lead sponsor
Association Française contre les Myopathies (AFM), Paris
Collaborator