Last reviewed · How we verify

NCT06256757

Safety and Validity of Extracorporeal Fenestration and in Situ Fenestration in Patients With Aortic Disease Involving the Left Subclavian Artery

Not yet recruiting NA Last updated 13 February 2024
What this trial tests

NA trial testing fenestration in Aortic Dissection Aneurysm in 170 participants. Not yet recruiting.

Timeline
1 May 2024
Primary endpoint
30 May 2028
30 April 2029

Quick facts

Lead sponsorThe Fourth Affiliated Hospital of Zhejiang University School of Medicine
PhaseNA
StatusNot yet recruiting
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment170
Start date1 May 2024
Primary completion30 May 2028
Estimated completion30 April 2029

Drugs / interventions tested

Conditions studied

Sponsor

The Fourth Affiliated Hospital of Zhejiang University School of Medicine

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

This trial aims to demonstrate the safety and validity of extracorporeal fenestration and in situ fenestration in patients with aortic disease involving the left subclavian artery.

Publications & conference data

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

  1. Safety and validity of extracorporeal fenestration and in situ fenestration in patients with aortic disease involving the left subclavian artery: a prospective, single-center, randomized controlled study.
    Jia X, Wu J, Ding C, Lou Y. · · 2025 · PMID 39885531 · DOI 10.1186/s13063-025-08746-5

Verify or expand the search:

Other recruiting trials for Aortic Dissection Aneurysm

Currently open trials in the same condition.

Other The Fourth Affiliated Hospital of Zhejiang University School of Medicine 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/NCT06256757.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing