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NCT06062524
Guo's False Lumen Embolization : The First in Man Study of WeFlow-EndoSeal Aorta Vascular Plug System
NA trial testing Aorta Vascular Plug System in Aortic Dissection Aneurysm in 20 participants. Currently enrolling.
31 May 2026
Quick facts
| Lead sponsor | Hangzhou Endonom Medtech Co., Ltd. |
|---|---|
| Phase | NA |
| Status | Recruiting now |
| Study type | INTERVENTIONAL |
| Allocation | na |
| Design | single group |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 20 |
| Start date | 24 October 2023 |
| Primary completion | 31 May 2026 |
| Estimated completion | 31 May 2026 |
| Sites | 3 locations across China |
Drugs / interventions tested
- Aorta Vascular Plug System
Conditions studied
- Aortic Dissection Aneurysm — all drugs for Aortic Dissection Aneurysm →
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):
-
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:
- PubMed search for NCT06062524
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other Hangzhou Endonom Medtech Co., Ltd. trials
Trials by the same sponsor.
- NCT07170332 — ZIPPER™ Stent-Graft Trial for Aortic Arch Dissection · NA · not yet recruiting
- NCT06385379 — Guo's Aortic Arch Reconstruction: A Multicenter, Prospective Study of the Novel WeFlow-Tribranch System (GENIUS Study) · NA · recruiting
- NCT05872282 — Percutaneous Endovascular Arch Repair Trial (PEART) Study · NA · unknown
- NCT05754541 — Guo's Endovascular Aortic Arch Replacement of Aortic Dissection by WeFlow-Tribranch Endoprothesis: a Multicenter Pilot S · NA · unknown
- NCT05179967 — Safety and Efficacy Study of WeFlow-JAAA Stent Graft System for Complex Abdominal Aortic Aneurysm(GREAT Study) · NA · unknown
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT06062524 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Hangzhou Endonom Medtech Co., Ltd.
- Last refreshed: 22 May 2024
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.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing