Menu
Not yet recruiting NCT06276413

REgistRy BRAnch goRE EndopRosthEsis

— Observational Aortic Aneurysm, Thoracic Aortic Dissection

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: GORE TAG Thoracic Branch Endoprosthesis.
Who it may be relevant to
Registry conditions: Aortic Aneurysm, Thoracic, Aortic Dissection. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Italy
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

Registry on Gore Branch Endoprosthesis

Overview

Multicenter registry on patients treated by the new Gore thoracic branched endoprosthesis

Detailed description

This is a multicenter, non-sponsored, physician-initiated multicenter registry on patients treated with the Gore thoracic branched endoprosthesis.

Inclusion of centers is on a voluntary basis; each participating center includes consecutive patients treated with this device.

Interventions

  • Device GORE TAG Thoracic Branch Endoprosthesis
    deployment of the GORE TAG Thoracic Branch Endoprosthesis fro thoraci aorta pathologies

Primary outcome measures

  • early mortality [Time frame: 30 days]
  • device stability [Time frame: 5 years]
  • technical success [Time frame: 30 days]
Secondary outcome measures (1)
  • early major adverse events [Time frame: 30 days]

Eligibility criteria

Inclusion criteria

  • patients receving the Gore TAG thoracic branched endograft for thoracic aorta pathologies

Exclusion criteria

  • less than 18 years
  • allergy to endograft components
  • patients receiving other types of arch endografts

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

Italy · 1 center
  • Vascular and Endovascular Clinic - Padova University — Padova

Identifiers

NCT: NCT06276413 · REBRA · REBRA

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗