Clinical trials

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Condition / disease
Location
Status: Recruiting

Further Evaluation of Safety and Performance of the NEXUS Aortic Arch Stent Graft System and the Custom-Made NEXUS Multibranch™ Aortic Arch Stent Graft System

The goal of this observational study is to collect clinical information on how safe, and how well the NEXUS Aortic Arch Stent Graft System and the Custom-Made NEXUS DUO™ Aortic Arch Stent Graft System work for the treatment of aortic aneurysms, in the standard-of-care setting. The main question\[s\] it aims to answer are: * Early mortality * Safety outcomes throughout the study * Device failure throughout the study * Procedural and hospitalisation information Participants will be treated per institutional standard of care Follow-up information will be collected through to five years.

Participants needed: 70
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Endospan Ltd.Updated: Dec 4, 2025Locations: 18
Eligibility criteria

Male and female age ≥18 years [+9]

Status: Recruiting

NEXUS Aortic Arch Clinical Study to Evaluate Safety and Effectiveness

Prospective, non-randomized, multi-center clinical investigation of the NEXUS™ Aortic Arch Stent Graft System (NEXUSTM) for the treatment of thoracic aortic lesions involving the aortic arch with a proximal landing zone, native or previously implanted surgical graft, in the ascending aorta and with a brachiocephalic trunk native landing zone.

Participants needed: 110
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Endospan Ltd.Updated: Oct 20, 2025Locations: 32
Eligibility criteria

Male and female age ≥ 18. [+30]

Acute dissection [+30]