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Randomized Comparison of DCB for the Treatment of Superficial Femoral and Popliteal Peripheral Artery Disease

NCT02648334 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 443

Last updated 2024-08-09

No results posted yet for this study

Summary

This study evaluates the safety and effectiveness Percutaneous Transluminal Angioplasty(PTA) using Drug-Coated Balloons for the treatment of Superficial Femoral and popliteal peripheral Artery disease.

Conditions

  • Angioplasty, Balloon
  • Catheterization, Peripheral
  • Popliteal Artery
  • Femoral Artery

Interventions

DEVICE

IN.PACT drug coated balloon

DEVICE

Lutonix drug coated balloon

Sponsors & Collaborators

  • Seung-Whan Lee, M.D., Ph.D.

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
19 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-11-10
Primary Completion
2023-01-19
Completion
2024-08-07

Countries

  • South Korea

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 NCT02648334 on ClinicalTrials.gov