PUlmonary REhabilitation in Patients Suffering From Post-PE Syndrome

Recruiting N/A Interventional Study
Pulmonary Embolism
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 – 90
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
48 (estimated)
Sponsor
Medical University of Vienna · Other
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About This Trial
This study is a multicenter, parallel, randomized waitlist-controlled trial that primarily focuses on the short-term benefit of outpatient pulmonary rehabilitation (PR) on patients after acute pulmonary embolism. Patients will be randomized into an intervention and a control group. The intervention group will receive 6 weeks of outpatient PR, while patients in the other treatment arm will serve a…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Post-PE syndrome (except patients previously diagnosed with CTEPH) diagnosed by any of the following: * Post-PE functional impairment criteria * Post-PE Cardiac Impairment criteria * Chronic Thromboembolic Disease criteria * Possibility of starting rehabilitation betwee…
Contacts

Stephan Nopp, Dr.

+43 40400 44170

stephan.nopp@meduniwien.ac.at

CONTACT