Viewing Study NCT04615130



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
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