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Trials / Recruiting

RecruitingNCT06055920

The PEERLESS II Study

PEERLESS II: RCT of FlowTriever vs. Anticoagulation Alone in Pulmonary Embolism

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
1,200 (estimated)
Sponsor
Inari Medical · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This study is a prospective, multicenter, randomized controlled trial of the FlowTriever System plus anticoagulation compared to anticoagulation alone for intermediate-risk acute PE.

Conditions

Interventions

TypeNameDescription
DEVICEFlowTriever SystemMechanical Thrombectomy for pulmonary embolism
DRUGAnticoagulation AgentsCommercially available/market approved anticoagulation medication including but not limited to: Heparin Sodium, Coumadin, Rivaroxaban, Apixaban, etc. Anticoagulants are a group of medications that decrease your blood's ability to clot.

Timeline

Start date
2023-11-17
Primary completion
2026-07-01
Completion
2026-07-01
First posted
2023-09-28
Last updated
2026-04-06

Locations

83 sites across 9 countries: United States, Belgium, Canada, Denmark, France, Germany, Poland, Spain, Switzerland

Regulatory

Source: ClinicalTrials.gov record NCT06055920. Inclusion in this directory is not an endorsement.

The PEERLESS II Study (NCT06055920) · Clinical Trials Directory