Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Novartis
Age
40–80
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Male and post-menopausal female adults aged 40-80 years inclusive.
Patients with a clinical diagnosis of COPD according to the Global Initiative for Chronic Lung Disease (GOLD) Guidelines (2005)
Smoking history of at least 10 pack years (either smokers or ex-smokers).
Able to perform reproducible spirometry maneuvers.
Able to communicate well with the investigator, to understand and comply with the requirements of the study. Understand and sign the written informed consent.
You may not be if
COPD exacerbations within 6 weeks prior to dosing
Concomitant lung disease such as asthma, requirement for long term oxygen treatment or history of lung reduction surgery.
Medical conditions that would interfere with the performance of spirometry or may pose a potential hazard from performing spirometry.
Any other medical condition that in the opinion of the Investigator may cause the patient to be unsuitable for completion of the study or place the patient at potential risk from being in the study, e.g. uncontrolled hypertension, unstable ischemic heart disease.
Participation in any clinical investigation within 4 weeks prior to dosing or longer if required by local regulations, and for any other limitation of participation based on local regulations.
Clareo Health | Effect of Indacaterol on Inspiratory Capacity and Lung Function in Patients With COPD Versus Placebo and Formoterol
