Pulmonary Hypertension Clinical Trial
Official title:
Study to Assess the Compliance of Patients With Pulmonary Arterial Hypertension Treated With Inhaled Iloprost.
This pilot, non-interventional, company-sponsored, multi-center study documents observational
data on patients under routine treatment of Pulmonary Arterial Hypertension (PAH) with
inhaled iloprost (using I-Neb device for the inhalation).
The planned study recruitment time is 18 months. The maximum follow up period in this study
will be 12 months.
The data will be collected from patients who have initiated the treatment mentioned above
(inhaled iloprost using I-Neb device) since February 1st, 2013.
Frequency of visits and procedures will be performed under routine conditions. The primary
objective of this study is to assess the compliance of patients with WHO/NYHA (World Health
Organization/New York Heart Association) functional Class III Pulmonary Arterial Hypertension
treated with Inhaled Iloprost in clinical practice, using the I-neb Insight tool.
n/a
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