Remedy, Biodegradable Peripheral Stent Registry

NCT01420120 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 100

Last updated 2015-07-16

No results posted yet for this study

Summary

This is a prospective multicenter registry to evaluate safety and performance of the REMEDY, biodegradable peripheral stent for the treatment of occluded or stenotic superficial femoral arteries. Patients will be followed for a period of 1 year.

Conditions

  • Peripheral Arterial Disease

Sponsors & Collaborators

  • be Medical

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-01-31
Primary Completion
2014-09-30
Completion
2014-09-30

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 NCT01420120 on ClinicalTrials.gov