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Endovascular Treatment of Peripheral Artery Disease

NCT03346577 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 60

Last updated 2021-01-14

No results posted yet for this study

Summary

The purpose of this observational study is to evaluate the performance and safety of endovascular treatment with stenting (Optimed Sinus Superflex 635) or balloon angioplasty (Cardionovum Legflow or Optimed Nylotrack .035 + .018) according to current practice. The goal of the study will be achieved by assessing binary restenosis with duplex ultrasound, peri- and postoperative complications, technical success, target lesion revascularization, amputation and clinical outcome.

Conditions

  • Peripheral Arterial Disease
  • Iliac Artery Disease
  • Below-the-knee Obstruction
  • Femoropopliteal Occlusive Disease

Interventions

DEVICE

stent or balloon

Endovascular treatment with stent or balloon according to current practice

Sponsors & Collaborators

  • be Medical

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-05-02
Primary Completion
2020-10-01
Completion
2020-10-01

Countries

  • Belgium

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 NCT03346577 on ClinicalTrials.gov