MN4000 for Treatment of CF and MND Patients in the Home Setting

NACompletedINTERVENTIONAL
Enrollment

10

Participants

Timeline

Start Date

March 9, 2017

Primary Completion Date

November 30, 2017

Study Completion Date

November 30, 2017

Conditions
Cystic FibrosisMotor Neuron DiseaseAirway Clearance Impairment
Interventions
DEVICE

MN 4000

Patients who required regular home airway clearance therapy were enrolled in the study and were prescribed therapy with the MN4000. Adherence to the prescribed therapy regimen and patient/caregiver satisfaction with the therapy was assessed. Pulmonary function, was assessed for each subject at baseline, after 1 month and after 3 months of home therapy. Results from the therapy period was compared to the baseline period, during which the subject received their regular airway clearance regimen. Airway Clearance Satisfaction surveys were conducted at baseline, after 1 month, and after 3 months of therapy. Results from the MN4000 therapy period were compared to the baseline period, during which the subject received their regular regimen

Trial Locations (1)

60208

Northwestern, Chicago

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Hill-Rom

INDUSTRY