The PERSEVERE Study: FlowTriever System for High-Risk Pulmonary Embolism
This study, called The PERSEVERE Study, is looking at a new way to treat high-risk pulmonary embolism (a blood clot in the lung). It compares the FlowTriever System, a device that removes blood clots, with the standard of care treatment. You might be able to join if you are at least 18 years old, have a blood clot in a main or lobar pulmonary artery, and have high-risk pulmonary embolism with right ventricle (RV) dysfunction (meaning the right side of your heart isn't pumping as well as it should). The study will measure how well these treatments work by looking at a combination of important health events, measured at hospital discharge or within 7 days. The current recruitment status is unclear.
- Study design
- This is a randomized controlled trial, meaning participants will be randomly assigned to receive either the FlowTriever System or standard of care. The study plans to enroll 200 participants.
- What's involved
- Not specified in the trial record.
- Compensation
- Not stated in the trial record.
- Follow-up
- The primary outcomes are measured at the earlier of initial hospital discharge or 7 days after randomization.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
The PERSEVERE Study
At a glance
Conditions
NCT06588634
Where you'd take part
This study runs at 29 sites. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.
AdventHealth Orlando
Orlando, Floridano site contact published
Recruiting
Allegheny General Hospital
Pittsburgh, Pennsylvaniano site contact published
Recruiting
Besançon University Hospital
Besançon, Franceno site contact published
Recruiting
CHU Grenoble Alpes
La Tronche, Franceno site contact published
Recruiting
CHU Nîmes Caremeau
Nîmes, Franceno site contact published
Recruiting
Emory University
Atlanta, Georgiano site contact published
Recruiting
HCA Medical City Heart & Spine
Dallas, Texasno site contact published
Recruiting
HCA Methodist Health San Antonio
San Antonio, Texasno site contact published
Recruiting
Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.
Study leadership
- Nicolas Meneveau, MD PhD · PRINCIPAL_INVESTIGATOR · Centre Hospitalier Universitaire Hôpital Jean Minjoz, Besançon, France
- John M Moriarty, MD · PRINCIPAL_INVESTIGATOR · Westwood Imaging Center & Interventional Radiology Clinic - UCLA, CA, USA
- Jay Giri, MD, MPH · PRINCIPAL_INVESTIGATOR · Penn Medicine, Philadelphia, PA, USA
Who to contact
Opens a ready-to-send draft in your own email app — review before sending.
What this trial measures
- Composite clinical endpoint of the following adjudicated events:The earlier of initial hospital discharge or 7 days after randomization
1. All-cause mortality 2. Cardiac arrest 3. Bailout to an alternative therapeutic strategy 4. Major bleeding 5. ECMO life support