Polygraphy at Home for Neuromuscular Patients Under Non-invasive Mechanical Ventilation
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).
| Condition(s) | Neuromuscular Diseases |
|---|---|
| Status | Recruiting |
| Study type | Observational |
| Summary | 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). |
| Who can participate | Inclusion Criteria: * 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. Exclusion Criteria: * Patient refusal; * Patient under guardianship; * Patient under AME scheme; * Patients living more than 40 km from reference center; * Patient depending on mechanical ventilation (more than 6 hours daily); * Rapidly or reversible evolutive neuro-myopathy (Amyotrophic lateral sclerosis, Guillain Barré syndrome, myasthenia). |
| Ages | 18 Years |
| Sex | All |
| Lead sponsor | Assistance Publique - Hôpitaux de Paris |
| Locations | Garches, France |
| Start date | 2024-03-08 |
| NCT ID | NCT05785637 |
| Official listing | https://clinicaltrials.gov/study/NCT05785637 |