Safety and Performance of the Zeus CC Stent for the Treatment of Iliac Occlusive Disease

NCT01499329 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 200

Last updated 2015-07-16

No results posted yet for this study

Summary

The purpose of this study is to evaluate safety and performance of the balloon-expandable Zeus CC (Rontis AG) stent for the treatment of Trans-Atlantic Inter-Society Consensus (TASC) A, B, C and D iliac lesions.

Conditions

Sponsors & Collaborators

  • be Medical

    lead INDUSTRY

Principal Investigators

  • Jan De Letter, MD · AZ Sint Jan Bruges

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-12-31
Primary Completion
2015-12-31
Completion
2015-12-31

Countries

  • Belgium

Study Locations

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Entities

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 NCT01499329 on ClinicalTrials.gov