Post-market Observational Study Zenith® t-Branch™

Post-market Observational Study Zenith® t-Branch™ Thoracoabdominal Endovascular Graft

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT02104089

Enrollment

Registered

2014-04-04

Start date

2014-01-31

Completion date

2020-01-09

Last updated

2020-01-27

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

Conditions

Aortic Aneurysm, Thoracoabdominal

Keywords

Thoracoabdominal aortic aneurysm, Endovascular, Fenestration, Branch, Off-the-shelf

Brief summary

The Zenith® t-Branch™ Thoracoabdominal Endovascular Graft Study is a post-market observational study to evaluate the performance of the Zenith® t-Branch™ in the treatment of thoracoabdominal aortic aneurysms in routine care.

Detailed description

Both retrospective and prospective patients will be enrolled

Interventions

DEVICEZenith® t-Branch™ Thoracoabdominal Endovascular Graft

Instead of making a large incision in the chest, the physician makes a small incision near each hip to insert, and guide the study device(s) into place in the aorta.

Study design

Observational model

CASE_ONLY

Time perspective

OTHER

Eligibility

Sex/Gender

ALL

Healthy volunteers

Inclusion criteria

* Treated with the off-the-shelf Zenith® t-Branch™ Thoracoabdominal Endovascular Graft * Signed informed consent

Exclusion criteria

* Inability or refusal to give informed consent by the patient or a legally authorized representative

Design outcomes

Primary

Measure	Time frame
Rate of mortality and morbidity	30 days

Countries

Germany, Sweden

Outcome results

None listed

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