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

JOTEC

Status: Completed

Conditions: Vascular Diseases

Treatments: Device: Surgical repair

Study type: Observational

Funder types: Industry

Identifiers

NCT04058691

FEOR

Details and patient eligibility

About

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).

Full 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.

Enrollment: 100 patients

Sex: All

Volunteers: No Healthy Volunteers

Inclusion criteria

None

Exclusion criteria

None