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

NCT04058691 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 100

Last updated 2023-01-25

No results posted yet for this study

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).

Conditions

  • Vascular Diseases

Interventions

DEVICE

Surgical repair

Open surgery

Sponsors & Collaborators

  • JOTEC GmbH

    lead INDUSTRY

Principal Investigators

  • Jean-Philippe Verhoye, Prof. · Rennes Pontchaillou University Medical Centre

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-11-01
Primary Completion
2020-02-20
Completion
2022-09-30

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04058691 on ClinicalTrials.gov