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Popliteal Artery Occlusion clinical trials

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NCT ID: NCT02813577 Terminated - Clinical trials for Femoral Artery Occlusion

Lutonix Drug Coated Balloon for Treatment of Femoropopliteal Arteries in United States Females (CONFIRM)

CONFIRM
Start date: April 20, 2018
Phase: N/A
Study type: Interventional

The post approval study will enroll US female patients presenting with claudication or ischemic rest pain and an angiographically significant lesion in the superficial femoral or popliteal artery. Subjects are treated per Instructions For Use (IFU) with the Lutonix® Catheter. Subjects will have a Duplex Ultrasound (DUS) and clinical follow-up through two (2) years.