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Prospective/Retrospective Registry of the E-vita OPEN PLUS Stent Graft System in France — FEOR  

Vascular Diseases Clinical Trial

Official title:
Prospective/Retrospective Multicenter Registry to Examine the Real-world Performance in France of the E-vita OPEN PLUS Stent Graft System

Clinical Trial Summary

The FEOR registry is undertaken to examine the real-world data of patients that were treated with the E-vita OPEN Plus Stent Graft System under routine care in France. This registry is a requirement of the Haute Autorité de Santé (HAS).

Clinical Trial Description

Data Collection on patients who have been implanted with an E-vita OPEN PLUS Stent Graft System from 15th July 2014 until 31st May 2019. The E-vita OPEN PLUS Stent Graft System was implanted at the discretion of the treating physician. Participating physicians provided their observations collected during routine care for patients he/she had decided to treat with the E-vita OPEN PLUS Stent Graft System. The period of data collection was three years starting from the intervention of each patient. Data verification was performed. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04058691
Study type Observational
Source JOTEC GmbH
Contact
Status Completed
Phase
Start date November 1, 2019
Completion date September 30, 2022
View Details
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