Investigation of Outpatient PUlmonary REhabilitation in Patients Suffering From Post-PE Syndrome: a Randomized Waitlist-controlled Trial - the PURE-PE Study

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

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 as a control. After completion of the randomized study, the second arm will undergo PR as well.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 90
Healthy Volunteers: f
View:

• 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 between 12 and 36 weeks after the initial event of PE

Locations
Other Locations
Austria
Therme Wien Med
RECRUITING
Vienna
Contact Information
Primary
Stephan Nopp, Dr.
stephan.nopp@meduniwien.ac.at
+43 40400 44170
Time Frame
Start Date: 2021-06-01
Estimated Completion Date: 2027-12-31
Participants
Target number of participants: 48
Treatments
Experimental: Intervention
Patients will undergo 6 weeks of outpatient rehabilitation.
No_intervention: Control
Patients will receive no intervention throughout the 6 weeks period.
Related Therapeutic Areas
Sponsors
Leads: Medical University of Vienna

This content was sourced from clinicaltrials.gov