Instrumental and Manual Increase of Couch in Neuromuscular Patients
NCT01518439 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20
Last updated 2013-07-19
Summary
Inefficient cough is responsible of respiratory complications in neuromuscular patients which can lead to hospitalisation and can be life threatening. Techniques enhancing cough efficiency are successful in improving the clearance of bronchial secretions and help non invasive ventilation efficiency especially in case of acute respiratory failure. Combining mechanical exsufflation to the manual techniques of physiotherapy might enhance efficiency. Therefore the investigators want to compare cough efficiency under different techniques of instrumental and manual of cough assistance in order to determine the best combination to optimize cough flow.
Conditions
- Neuromuscular Disease
- Chronic Respiratory Failure
- Coughing
Interventions
- DEVICE
-
Alpha 200®
inspiratory capacity is increased with the use of constant pressure device: Alpha 200®
- DEVICE
-
Alpha 200® + physiotherapist
inspiratory capacity is increased with the use of constant pressure device (Alpha 200®) combined with the manual pressures techniques to increase cough by the physiotherapist
- DEVICE
-
Cough Assist®
increased inspiratory capacity and mechanical exsufflation with the use of insufflation-exsufflation device (Cough Assist®)
- DEVICE
-
Cough Assist® + physiotherapist
increased inspiratory capacity and mechanical exsufflation with the use of insufflation-exsufflation device (Cough Assist®) combined with the manual pressures techniques to increase cough by the physiotherapist
- OTHER
-
physiotherapist
manual pressures techniques to increase cough applied by the physiotherapist
Sponsors & Collaborators
-
Adep Assistance
collaborator OTHER -
Centre d'Investigation Clinique et Technologique 805
lead OTHER
Principal Investigators
-
Frederic Lofaso, Md-PhD · University of Versailles
-
Helene Prigent, MD-PhD · University of Versailles
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2012-01-31
- Primary Completion
- 2012-01-31
- Completion
- 2013-07-31
Countries
- France
Study Locations
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