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An Observational Study to Evaluate Safety, Performance, and Clinical Benefit of BeFlow

NCT07010354 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 100

Last updated 2025-09-19

No results posted yet for this study

Summary

This international, observational multi-centre study of the device BFI will monitor technical success of the implantation, data regarding clinical performance, clinical benefit, as well as potential unknown side effects pursuant to the Intended Purpose.

Conditions

  • Iliac Artery Stenosis
  • Iliac Artery Occlusion

Interventions

DEVICE

Stenting

Endovascular treatment of stenosed or occluded iliac arteries: Permanent intraluminal placement of a covered stent

Sponsors & Collaborators

  • ID3 Medical

    collaborator OTHER

  • Bentley InnoMed GmbH

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-08-08
Primary Completion
2026-07-31
Completion
2031-07-31

Countries

  • Belgium
  • Switzerland

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 NCT07010354 on ClinicalTrials.gov