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Evaluation of the iCover Stent as a Bridging Stent in Fenestrated Endovascular Aneurysm Repair (fEVAR) for Complex Aortic Aneurysms.

NCT07742254 · Status: ENROLLING_BY_INVITATION · Type: OBSERVATIONAL · Enrollment: 154

Last updated 2026-08-03

No results posted yet for this study

Summary

ReiCo is a French retrospective, multicenter, single-arm study focused on assessing the safety and clinical performance of the iCover balloon-expandable covered stent (iVascular) when implanted as a bridging stent during fEVAR for complex abdominal aortic aneurysms. The aim is to demonstrate conformity by collecting clinical evidence supporting the safe and effective use of this device in fEVAR procedures.

Conditions

  • Aortic Aneurysm
  • Aortic Aneurysm Abdominal

Sponsors & Collaborators

  • iVascular S.L.U.

    lead INDUSTRY

Principal Investigators

  • Sara Pich, phD · iVascular

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-03-06
Primary Completion
2026-07-31
Completion
2026-08-30

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 NCT07742254 on ClinicalTrials.gov