Ignite Creation Date:
2024-05-06 @ 3:23 PM
Last Modification Date:
2024-10-26 @ 1:48 PM
Study NCT ID:
NCT04615130
Status:
RECRUITING
Last Update Posted:
2024-03-22
First Post:
2020-10-22
Brief Title:
PUlmonary REhabilitation in Patients Suffering From Post-PE Syndrome
Sponsor:
Medical University of Vienna
Organization:
Medical University of Vienna
Study Overview
Official Title:
Investigation of Outpatient PUlmonary REhabilitation in Patients Suffering From Post-PE Syndrome a Randomized Waitlist-controlled Trial - the PURE-PE Study
Status:
RECRUITING
Status Verified Date:
2024-03
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
PURE-PE
Brief 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
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
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None