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NCT06576427 · ClinicalTrials.gov registry record · NA

Selective Pulmonary-artery Intervention to Reduce Acute Right-heart tEnsion-II

A NA study of Pulmonary Embolism, sponsored by Jupiter Endovascular.

Active
Registry status
NA
Development phase
123
Enrollment target
20
Study locations

NCT06576427 is a NA study of Pulmonary Embolism that is active but no longer recruiting, run by Jupiter Endovascular. The registered enrollment target is 123 participants, below the 3,056-participant average among 48 other Pulmonary Embolism trials with a reported enrollment target (96% lower). The trial reports 20 study locations across 12 states.

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The verdict

NCT06576427, a NA study of Pulmonary Embolism, is active but no longer recruiting, sponsored by Jupiter Endovascular.

ACTIVE NOT RECRUITING
Registry status
NA
Development phase
123 participants
Enrollment target
20
Study locations

Study Summary

This study is a prospective, single-arm, multicenter study to evaluate the safety and effectiveness of the Vertex Pulmonary Embolectomy System in participants presenting with clinical signs and symptoms of acute pulmonary embolism.

Conditions Studied

Interventions

  • DEVICE Vertex Pulmonary Embolectomy System

Study Locations (20)

New York

  • NYU Langone Health - New York
  • Northwell Health - Staten Island
  • Westchester Medical Center - Valhalla

North Carolina

  • University of North Carolina - Chapel Hill
  • Duke University - Durham
  • Wake Forest Medical Center - Winston-Salem

Pennsylvania

  • Penn Presbyterian - Philadelphia
  • UPMC Presbyterian - Pittsburgh
  • St Clair Health - Pittsburgh

Michigan

  • Henry Ford Hospital - Detroit
  • Henry Ford St John - Detroit

Other

  • Medical University of Vienna - Vienna
  • St. John Paul II Hospital - Krakow

Connecticut

  • Hartford Hospital - Hartford

Florida

  • Ascension Sacred Heart - Pensacola

Georgia

  • Emory University - Atlanta

Trial Details

FieldValue
Enrollment Target 123 participants
Start Date 2024-10-15
Est. Completion 2026-03
Phase NA

Sponsor

Jupiter Endovascular

1 total trials

What the Registry Record Tells You About NCT06576427

The ClinicalTrials.gov registry entry for NCT06576427 describes a study currently listed as active not recruiting, categorized as NA. The registered enrollment target is 123 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 3,056-participant average among 48 other Pulmonary Embolism trials with a reported enrollment target (96% lower). The listed sponsor is Jupiter Endovascular, which has 1 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Pulmonary Embolism appearing as the primary indexed condition, and to 1 intervention - of which Vertex Pulmonary Embolectomy System is the first listed.

NCT06576427 reports 20 study locations spanning 12 distinct geographic areas - top geographies include New York, North Carolina, Pennsylvania.

Frequently Asked Questions

What is clinical trial NCT06576427 about?

NCT06576427 is a clinical study titled "Selective Pulmonary-artery Intervention to Reduce Acute Right-heart tEnsion-II". This study is a prospective, single-arm, multicenter study to evaluate the safety and effectiveness of the Vertex Pulmonary Embolectomy System in participants presenting with clinical signs and symptoms of acute pulmonary embolism.

What is the current status of trial NCT06576427?

This trial is currently active not recruiting. It is a NA study. The enrollment target is 123 participants. The study started on 2024-10-15. Estimated completion is 2026-03.

What conditions does trial NCT06576427 study?

This clinical trial studies the following conditions: Pulmonary Embolism.

What interventions are being tested in trial NCT06576427?

The interventions under investigation include: Vertex Pulmonary Embolectomy System (DEVICE).

Who is sponsoring clinical trial NCT06576427?

This trial is sponsored by Jupiter Endovascular, which has 1 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06576427 being conducted?

This trial has 20 study locations across Connecticut, Florida, Georgia, Michigan, New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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