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Clinical Trial Summary

Patients with peripheral artery disease will be treated with either drug coated balloon catheter, drug coated stent or uncoated stent.


Clinical Trial Description

Patients with chronic stenotic or occlusive atherosclerotic disease and lesions of at least 13 cm length in the SFA or Arteria poplitea segment 1 will be randomized to either treatment with paclitaxel coated balloon catheter, paclitaxel coated stent or bare nitinol stent. Vessel patency will be evaluated by quantitative angiography after 12 months. Clinical follow-ups will be done until 36 months post-intervention. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03332264
Study type Interventional
Source InnoRa GmbH
Contact
Status Completed
Phase N/A
Start date March 30, 2017
Completion date December 12, 2023

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