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Evaluation of the GORE® VIABAHN® Endoprosthesis for the Treatment of Popliteal Artery Aneurysm (PAA)

NCT02462876 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 60

Last updated 2022-03-28

Study results available
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Summary

This study will assess the long term safety and performance of the GORE® VIABAHN® Endoprosthesis for the treatment of patients with Popliteal Artery Aneurysms.

Conditions

  • Popliteal Artery Aneurysm

Interventions

DEVICE

GORE® VIABAHN® Endoprosthesis

Treatment of Popliteal Artery Aneurysm with the GORE® VIABAHN® Endoprosthesis.

Sponsors & Collaborators

  • W.L.Gore & Associates

    lead INDUSTRY

Principal Investigators

  • Nabil Chakfé · Hôpitaux Universitaire de Strasbourg

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-10-31
Primary Completion
2018-07-31
Completion
2020-12-31

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 NCT02462876 on ClinicalTrials.gov