MedTrace Logo

BGP Stent as Bridging Stent in FEVAR

NCT03987035 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 103

Last updated 2025-04-09

No results posted yet for this study

Summary

The objective of this clinical investigation is to evaluate, in a controlled setting, the safety and performance of the BeGraft Peripheral (BGP) balloon expandable covered stent Graft System (Bentley InnoMed, Hechingen, Germany) implanted as bridging stent in FEVAR (fenestrated endovascular aortic repair) for complex aortic aneurysms.

Conditions

  • Thoracoabdominal Aortic Aneurysm, Without Mention of Rupture
  • Abdominal Aortic Aneurysm, Without Mention of Rupture

Interventions

DEVICE

BeGraft Peripheral (BGP) Stent Graft System as bridging stent

BGP Stent Graft System as bridging stent

Sponsors & Collaborators

  • Marc Bosiers, MD

    lead OTHER

Principal Investigators

  • Eric Verhoeven, Prof. Dr. · Foundation for Cardiovascular Research and Education

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
55 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-03-18
Primary Completion
2022-07-19
Completion
2024-08-31

Countries

  • Germany

Study Locations

More Related Trials

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 NCT03987035 on ClinicalTrials.gov