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DANCE Partner: Inflammatory Biomarker Analysis by Femoropopliteal Revascularization Method and Treatment Outcomes

NCT02469532 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 31

Last updated 2018-03-08

No results posted yet for this study

Summary

This is a prospective, multi-center, observational registry to document the baseline, 24-hour and 30-day inflammatory response and procedural outcomes out to 12 month follow-up after femoropopliteal angioplasty or atherectomy-based revascularization procedures.

Conditions

  • Peripheral Arterial Disease

Interventions

DEVICE

Balloon Angioplasty

Device: Balloon Angioplasty Selection is driven by preference of the operator

DEVICE

Atherectomy System

Device: Orbital or Directional or Laser Atherectomy Systems Atherectomy selection is driven by preference of the operator

Sponsors & Collaborators

  • Mercator MedSystems, Inc.

    lead INDUSTRY

Principal Investigators

  • Jason A Yoho, MD · Mission Research, New Braunfels, TX

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-05-31
Primary Completion
2017-10-31
Completion
2018-01-31

Countries

  • United States

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 NCT02469532 on ClinicalTrials.gov