50
Participants
Start Date
June 30, 2016
Primary Completion Date
November 30, 2018
Study Completion Date
November 30, 2018
Ultibro®
The intervention in this arm is the Ultibro®. To keep the patients blinded on which treatement they are taking they will use the two devices but in this arm the Ultibro will be delivered and the Spiriva will be a placebo. We will measure the exertional dyspnea after 21 days of treatment.
Spiriva®
The intervention in this arm is the Spiriva®. To keep the patients blinded on which treatement they are taking they will use the two devices but in this arm the Ultibro will be a placebo and the Spiriva will be delivered. We will measure the exertional dyspnea after 21 days of treatment.
Queens University, Kingston
McGill University, Montreal
Laval University - IUCPQ, Québec
Collaborators (1)
Novartis
INDUSTRY
Laval University
OTHER