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NCT06062524

Guo's False Lumen Embolization : The First in Man Study of WeFlow-EndoSeal Aorta Vascular Plug System

Recruiting now NA Last updated 22 May 2024
What this trial tests

NA trial testing Aorta Vascular Plug System in Aortic Dissection Aneurysm in 20 participants. Currently enrolling.

Timeline
24 October 2023
Primary endpoint
31 May 2026
31 May 2026

Quick facts

Lead sponsorHangzhou Endonom Medtech Co., Ltd.
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment20
Start date24 October 2023
Primary completion31 May 2026
Estimated completion31 May 2026
Sites3 locations across China

Drugs / interventions tested

Conditions studied

Sponsor

Hangzhou Endonom Medtech Co., Ltd.

Who can join

Adults 18 to 80, any sex, with Aortic Dissection Aneurysm. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

A prospective, single-center, first in man study to evaluate the safety and efficacy of WeFlow-EndoSeal Aorta Vascular Plug System manufactured by Hangzhou Endonom Medtech Co., Ltd. for the dissecting aneurysm of descending thoracic aorta after aortic dissection repair.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. First in man: blocking the false lumen backflow of aortic dissection after thoracic endovascular aortic repair by an off-the-shelf EndoSeal™ system.
    Ge Y, Zhang H, Guo W. · · 2024 · cited 4× · PMID 38427788 · DOI 10.1093/eurheartj/ehae117

Verify or expand the search:

Other Hangzhou Endonom Medtech Co., Ltd. trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06062524.

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