Informations générales (source: ClinicalTrials.gov)
Factors Associated With Hypoventilation in the Myotonic Dystrophy, Progressive Profile Over 5 Years (Steinert)
Observational
University Hospital, Lille (Voir sur ClinicalTrials)
juin 2010
septembre 2023
29 juin 2024
The aim of this study is to determine the factors associated with alveolar
hypoventilation in terms of cognitive impairment, daytime sleepiness, respiratory
function, nocturnal respiratory events This evaluation will clarify the clinical
phenotypes of respiratory disease in myotonic steinert dystrophy.
Etablissements
Les établissements d'Île-de-France dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données | |||||
---|---|---|---|---|---|
AP-HP - Hôpital La Pitié-Salpêtrière | Contact (sur clinicalTrials) | ||||
AP-HP - Hôpital Raymond Poincaré | Contact (sur clinicalTrials) | ||||
Les établissements hors Île-de-France dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données | |||||
Chu de Nantes :Site Hôtel-Dieu- Hme - Nantes 1 - Nantes - France | Contact (sur clinicalTrials) | ||||
Les établissements sans correspondance certaine dans le répertoire FINESS dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données | |||||
Centre Hospitalier Regional D' Angers - Angers - France | Contact (sur clinicalTrials) | ||||
Chu Montpellier - Montpellier - France | Contact (sur clinicalTrials) | ||||
Hôpital Calmette, CHRU - Lille - France | Contact (sur clinicalTrials) |
Critères
Tous
Inclusion Criteria:
- Myotonic dystrophy of Steinert genetically confirmed (number of known CTG repeats),
in its classical form of adult
- Myotonic dystrophy of Steinert genetically confirmed (number of known CTG repeats),
in its classical form of adult
- Inability to perform EFR assessment or polysomnography
- Moderate to severe asthma according to the GINA classification
- moderate to severe COPD (> stage 1 of the GOLD recommendations)
- Other significant respiratory pathology
- Patient already on NIV, CPAP or under oxygen therapy
- Impossibility of receiving enlightened information
- Inability to participate in the entire study