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EVUS guided wiring vs. knuckle wiring for femoropopliteal chronic total occlusive lesio

Not Applicable
Recruiting
Conditions
peripheral artery disease
Registration Number
JPRN-UMIN000045983
Lead Sponsor
Toyohashi heart center
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
200
Inclusion Criteria

Not provided

Exclusion Criteria

1) Patients with acute lower limb ischemia or acute thrombosis 2) Patients with a history of stent placement for the target blood vessel 3) Patients with non-arteriosclerotic stenosis and obstructive lesions 4) Patients who have difficulty taking antiplatelet drugs / anticoagulants 5) Chronic limb threatening ischemia (CLTI) Rutherford classification 5 or 6 6) When the doctor in charge judges that it is inappropriate 7) Cases in which blood vessels cannot be visualized with EVUS

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Primary patency rate (at 1 month, 6 months, 12 months, 18 months, 24 months, 36 months, 48 months, 60 months)
Secondary Outcome Measures
NameTimeMethod
Freedom from TLR MACLE Wire passage route evaluated by IVUS Degree of dissection after balloon dilation, angiographic findings, IVUS findings Procedure time, radiation exposure, contrast medium usage Procedure complications Improvement of patient symptoms by Rutherford classification Improvement of ABI
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