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NCT07089576 · ClinicalTrials.gov registry record · NA

Clinical Study to Evaluate the Safety and Effectiveness of Arcevo LSA

A NA study of Aortic Arch Aneurysm and Aortic Arch Dissection, sponsored by Artivion.

Recruiting
Registry status
NA
Development phase
132
Enrollment target
10
Study locations

NCT07089576: Recruiting NA study of Aortic Arch Aneurysm and Aortic Arch Dissection, sponsored by Artivion.

NCT07089576 is a NA study of Aortic Arch Aneurysm and Aortic Arch Dissection that is actively recruiting participants, run by Artivion. The registered enrollment target is 132 participants, below the 501-participant average among 4 other Aortic Arch Aneurysm trials with a reported enrollment target (74% lower). The trial reports 10 study locations across 8 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT07089576, a NA study of Aortic Arch Aneurysm and Aortic Arch Dissection, is actively recruiting participants, sponsored by Artivion.

RECRUITING
Registry status
NA
Development phase
132 participants
Enrollment target
10
Study locations

Study Summary

The goal of this clinical trial is to learn if the Arcevo LSA stent graft can safely and effectively treat patients that have an acute or chronic aortic dissection and/or aneurysm that involves the aortic arch and the descending thoracic aorta, with or without the involvement of the ascending aorta.

Primary Outcome

The major adverse events included in the composite are: * All-cause mortality * New permanent disabling stroke * New permanent paraplegia and/or paraparesis * Unanticipated aortic reoperation in the treated segment * LSA occlusion

Interventions

  • DEVICE Arcevo™ LSA Hybrid Stent Graft System

Study Locations (10)

New York

  • Columbia University Irving Medical Center/New York Presbyterian Hospital - New York
  • Montefiore Medical Center - The Bronx

Texas

  • University of Texas - Austin - Austin
  • Baylor Scott & White - Plano

California

  • University of Southern California - Los Angeles

Georgia

  • Emory University School of Medicine - Atlanta

Illinois

  • Northwestern University Feinberg School of Medicine - Chicago

Maryland

  • Johns Hopkins Hospital - Baltimore

Ohio

  • Cleveland Clinic Foundation - Cleveland

Wisconsin

  • Medical College of Wisconsin - Milwaukee

Trial Details

FieldValue
Enrollment Target 132 participants
Start Date 2025-11-04
Est. Completion 2032-07
Phase NA
Artivion

7 total trials

What NCT07089576 shows while recruiting

NCT07089576 is an interventional study that assigns participants to a tested intervention. The registered 132 participants enrollment target is mid-sized for trials with a published cap, below the 501-participant average among 4 other Aortic Arch Aneurysm trials with a reported enrollment target (74% lower).

The record links to 4 conditions, with Aortic Arch Aneurysm appearing as the primary indexed condition, and to 1 intervention - of which Arcevo™ LSA Hybrid Stent Graft System is the first listed.

NCT07089576 lists 10 locations in 8 states (New York, Texas, California).

Frequently Asked Questions

What is clinical trial NCT07089576 about?

NCT07089576 is a clinical study titled "Clinical Study to Evaluate the Safety and Effectiveness of Arcevo LSA". The goal of this clinical trial is to learn if the Arcevo LSA stent graft can safely and effectively treat patients that have an acute or chronic aortic dissection and/or aneurysm that involves the aortic arch and the descending thoracic aorta, with or without the involvement of the ascending aorta.

What is the current status of trial NCT07089576?

This trial is currently recruiting. It is a NA study. The enrollment target is 132 participants. The study started on 2025-11-04. Estimated completion is 2032-07.

What conditions does trial NCT07089576 study?

This clinical trial studies the following conditions: Aortic Arch Aneurysm, Aortic Arch Dissection, Acute Aortic Dissection, Chronic Aortic Dissection.

What interventions are being tested in trial NCT07089576?

The interventions under investigation include: Arcevo™ LSA Hybrid Stent Graft System (DEVICE).

Who is sponsoring clinical trial NCT07089576?

This trial is sponsored by Artivion, which has 7 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07089576 being conducted?

This trial has 10 study locations across California, Georgia, Illinois, Maryland, New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Source: ClinicalTrials.gov NCT07089576, the US trial registry maintained by the National Library of Medicine. NCT07089576 (mid enrollment · multi site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.