Phase
Condition
Myasthenia Gravis (Chronic Weakness)
Amyotrophic Lateral Sclerosis (Als)
Scar Tissue
Treatment
MI-E without PEP function activated during the pause
MI-E with PEP function activated during the pause
Clinical Study ID
Ages 18-100 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Male or female patient aged over 18 years
Patient with Amyotrophic Lateral Sclerosis (ALS)
Patients with established or beginning bulbar disorders, identified by thehealthcare team (speech impairment, hypersalivation, or swallowing difficulties)
Patient naive to INEX therapy but prescribed for its installation or patient alreadytreated by an INEX device
Patient followed by the ALS mobile team of the Groupe Hospitalier du Havre or theCHU of Dijon
Patient whose disease progression kinetics is medically deemed compatible withinclusion in the study
Patient willing to participate in the research after receiving adequate informationand the information letter.
Patient affiliated with social security or a beneficiary of such a scheme.
Exclusion
Exclusion Criteria:
"● Patient not presenting an episode of infection or a past episode of respiratory infection less than one month old
Mental illness interfering with the proper use of the device
History of laryngospasm
Inability to come for consultation with the ALS team of the Groupe Hospitalier duHavre or the CHU of Dijon
Pregnancy
Person deprived of liberty by judicial or administrative decision, person subject toa legal protection measure (patient under guardianship or curatorship) ArticleL1121-8.
Appearance of a non-inclusion criterion
Refusal to participate after inclusion
Death from any cause"
Study Design
Study Description
Connect with a study center
GH Havre
Le Havre, Normandie 76290
FranceActive - Recruiting
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