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Clinical Trial Summary

The primary objective of this study is to evaluate the effect of selexipag on the physical activity of patients with pulmonary arterial hypertension (PAH) in their daily life, by using a wearable wrist device (actigraph). The actigraph will collect data on daily life physical activity in the patient's real environment. In addition, the PAH symptoms and their impacts will be assessed by using an electronic patient reported outcome measure in the patient's real environment. Patients will be assigned randomly to either selexipag or placebo.


Clinical Trial Description

This study is designed as exploratory with the purpose to generate hypotheses on new endpoints ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03078907
Study type Interventional
Source Actelion
Contact
Status Completed
Phase Phase 4
Start date November 8, 2017
Completion date February 10, 2020

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