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.

NCT06588634

The PERSEVERE Study

Recruiting
NAAges 18+InterventionalTreatment
Inari Medical
~200 participants
Updated 2026-09-11 on ClinicalTrials.gov
What's tested:FlowTriever SystemStandard of Care

At a glance

Recruiting sites
29 of 29 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Composite clinical endpoint of the following adjudicated events:
Measured over The earlier of initial hospital discharge or 7 days after randomization
Pulmonary Embolism
Pulmonary Thromboembolism

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.

  • 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

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  • 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