FlowTriever Pulmonary Embolectomy Clinical Study - FlowTriever2

Status: Completed
Location: See all (7) locations...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The FLARE-FT2 confirmatory study is a prospective, single-arm, multicenter study of the FlowTriever2 Catheter for mechanical thrombectomy of pulmonary embolism (PE).

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 75
Healthy Volunteers: f
View:

• Clinical signs and symptoms consistent with acute PE

• PE symptom duration ≤ 14 days

• CTA evidence of proximal PE (filling defect in at least one main or lobar pulmonary artery)

• RV/LV ratio of ≥ 0.9 (NOTE: Enrollment qualification assessment based on Investigator's interpretation of RV/LV ratio)

• Systolic blood pressure ≥ 90 mmHg (initial SBP may be ≥ 80 mmHg if the pressure recovers to ≥ 90 mmHg with fluids)

• Stable heart rate \< 130 BPM prior to procedure

• Patient is deemed medically eligible for interventional procedure(s), per institutional guidelines and/or clinical judgment.

• FlowTriever2 Catheter enters the vasculature

Locations
United States
Arizona
Carondelet St. Joseph's Hospital
Tucson
Connecticut
Yale University
New Haven
Georgia
Memorial Health University Medical Center
Savannah
Kentucky
Baptist Health
Louisville
New Jersey
Virtua Health
Camden
Oklahoma
Oklahoma Heart Institute
Tulsa
Tennessee
University of Tennessee Medical Center
Knoxville
Time Frame
Start Date: 2023-02-14
Completion Date: 2024-09-09
Participants
Target number of participants: 50
Treatments
Experimental: All Subjects
All participants who were treated with the FlowTriever System and FlowTriever2 Catheter.
Sponsors
Leads: Inari Medical

This content was sourced from clinicaltrials.gov