Mid- and Long-term Outcomes of Custom-made Aortic Devices

Results From a Multicenter Registry on the Outcomes of the Terumo Custom-made Aortic Endograft

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT05777460

Enrollment

Registered

2023-03-21

Start date

2020-10-01

Completion date

2027-11-01

Last updated

2025-03-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Aortic Diseases, Thoracic Aortic Aneurysm

Brief summary

This study aims to evaluate mid- and long-term outcomes after Thoracic endovascular aortic repair (TEVAR) with custom-made devices.

Interventions

DEVICEThoracic endovascular aortic repair (TEVAR)

The TEVAR procedure involves the placement of a covered stent (a metal mesh tube with a layer of fabric) into the weakened area of the artery.

Study design

Observational model

COHORT

Time perspective

RETROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

* Thoracic Aortic Disease

Exclusion criteria

* Urgent/Emergent treatment

Design outcomes

Primary

Measure	Time frame	Description
Overall Mortality	3 years	Any death occurring during follow-up
Aortic-related mortality	3 years	Any death occurring during follow-up and related to the procedure

Countries

Italy

Contacts

Primary ContactGiovanni Tinelli

giovanni.tinelli@policlinicogemelli.it‭+39 347 4864020‬

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026