Prospective/Retrospective Registry of the E-vita OPEN PLUS Stent Graft System in France
Last updated on July 2021Recruitment
- Recruitment Status
- Active, not recruiting
- Estimated Enrollment
- Same as current
Summary
- Conditions
- Vascular Diseases
- Type
- Observational
- Design
- Observational Model: CohortTime Perspective: Retrospective
Participation Requirements
- Age
- Younger than 125 years
- Gender
- Both males and females
Description
In this registry data will be collected on patients who have been implanted with an E-vita OPEN PLUS Stent Graft System from 15th of July 2014 until May 31st 2019. The E-vita OPEN PLUS Stent Graft System will be implanted at the discretion of the treating physician. Participating physicians will be ...
In this registry data will be collected on patients who have been implanted with an E-vita OPEN PLUS Stent Graft System from 15th of July 2014 until May 31st 2019. The E-vita OPEN PLUS Stent Graft System will be implanted at the discretion of the treating physician. Participating physicians will be asked to provide their observations collected during routine care for patients he/she had decided to treat with the E-vita OPEN PLUS Stent Graft System. As this registry is a requirement of the Haute Autorité de Santé (HAS), written Informed consent of the patients is not required, however all patients will be provided with a non-objection letter and given the opportunity to refuse to participate. The period of data collection will be three years starting from the intervention of each patient. Data verification will be performed.
Tracking Information
- NCT #
- NCT04058691
- Collaborators
- Not Provided
- Investigators
- Principal Investigator: Jean-Philippe Verhoye, Prof. Rennes Pontchaillou University Medical Centre
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