In this 5-months study, the response of patients to salbutamol at baseline will be compared with their response to treatment with indacaterol.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
625
Indacaterol 150 µg once-daily via single-dose dry powder inhaler
Coefficient of correlation between FEV1 and reversibility
Coefficient of correlation between the change from baseline in FEV1 with indacaterol after 1 month and the reversibility to salbutamol at screening
Time frame: After 1 month
Coefficient of correlation between VQ11 (an assessment of quality of life) and reversibility
Coefficient of correlation between the change from baseline in VQ11 with indacaterol after 5 months and the reversibility to salbutamol at screening
Time frame: 5 months
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Novartis Investigative Site
Ferolles-Attily, France, France
Novartis Investigative Site
Suresnes, France, France
Novartis Investigative Site
Vernon, France, France
Novartis Investigative Site
Abbeville, France
Novartis Investigative Site
Ajaccio, France
Novartis Investigative Site
Albi, France
Novartis Investigative Site
Albi, France
Novartis Investigative Site
Amboise, France
Novartis Investigative Site
Amiens, France
Novartis Investigative Site
Amiens, France
...and 127 more locations