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Rapid Exchange Devices Observational Registry.

NCT01994798 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 525

Last updated 2016-04-26

No results posted yet for this study

Summary

This registry is designed to assess the clinically relevant benefits of balloon angioplasty and stenting in superficial femoral and popliteal artery, using rapid exchange technology.

Conditions

  • Peripheral (Lowr Extremity) Arterial Disease.

Sponsors & Collaborators

  • Terumo Europe N.V.

    lead INDUSTRY

Principal Investigators

  • Christophe Martinez · Centre Hospitalier Universitaire (CHU) Liège

  • Omar Andrés Navarro · Hospital Universitari Dr. Josep Trueta de Girona

  • Josua Van den Berg · Ospedale Regionale di Lugano

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-11-30
Primary Completion
2016-09-30
Completion
2016-12-31

Countries

  • Belgium
  • Spain

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 NCT01994798 on ClinicalTrials.gov