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Completed Not applicable Interventional

Endovascular Engineering ENGULF Study

ClinicalTrials.gov ID: NCT05597891

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This page only displays public information reproduced from the official ClinicalTrials.gov record NCT05597891. It adds no medical advice, opinions, or eligibility judgments. The official record remains the source of truth for eligibility criteria, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 15, 2026, 4:15 PM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Safety and Feasibility Single-Arm Study of a Novel Catheter Thrombectomy Device For the Treatment of Pulmonary Embolism (ENGULF)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Evaluation of initial safety and clinical feasibility of the Hēlo PE Thrombectomy System for thrombectomy in acute submassive pulmonary embolism (PE).

Study identification

NCT ID
NCT05597891
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Endovascular Engineering
Industry
Enrollment
177 participants

Conditions and interventions

Interventions

Device

Eligibility (public fields only)

Age range
18 Years to 90 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jan 12, 2023 (Actual)
Primary completion
Mar 2, 2026 (Actual)
Completion
Mar 30, 2026 (Actual)
Last update posted
Apr 14, 2026

2023 – 2026

United States locations

U.S. sites
21
U.S. states
10
U.S. cities
16
Facility City State ZIP Site status
PIH Health Good Samaritan Hospital Los Angeles California 90017 —
Huntington Hospital Pasadena California 91105 —
The Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center Torrance California 90502 —
Torrance Memorial Medical Center Torrance California 90505 —
Delray Medical Center Delray Beach Florida 33484 —
Baptist Health Research Institute Jacksonville Florida 32207 —
HCA Florida Memorial Hospital Jacksonville Florida 32216 —
Piedmont Heart Atlanta Georgia 30309 —
Northside Hospital Atlanta Georgia 30342 —
Indiana University Indianapolis Indiana 46202 —
Beth Israel Deaconess Medical Center Boston Massachusetts 02215 —
Brigham and Women's Hospital Boston Massachusetts 02215 —
TriHealth Hatton Research Institute Cincinnati Ohio 45242 —
University of Pennsylvania Philadelphia Pennsylvania 19104 —
Temple University Philadelphia Pennsylvania 19122 —
Wellmont Cardiology Services / Ballad Health Kingsport Tennessee 37660 —
Tennova Healthcare - Turkey Creek Medical Center Knoxville Tennessee 37934 —
Austin Heart Austin Texas 78705 —
Baylor Scott & White Research Institute Dallas Texas 75204 —
UT Health Houston Texas 77030 —
Gundersen Health La Crosse Wisconsin 54601 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05597891, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 14, 2026 · Synced Nov 15, 2026

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