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.
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