Open-label multicenter registry on the Outcomes of in-stent restenosis treated by Balloon angioplasty with Optical Frequency Domain Imaging in superficial femoral artery
Not Applicable
- Conditions
- peripheral arterial disease
- Registration Number
- JPRN-UMIN000021121
- Lead Sponsor
- Division of Cardiovascular Medicine, Department of Internal Medicine, Kobe University Graduate School of Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
Not provided
Exclusion Criteria
1)patients with in-stent occlusion in superficial femoral artery. 2)patients with all three occlusion artery below the knee 3)patients with uncontrollable heart failure 4)patients with acute limb ischemia or acute thrombotic occlusion 5)patients can not recieve antiplatelet therapy 6)female patients during pregnancy or breast-feeding 7)patients judged inappropriate for this study by physician
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Restenosis with duplex ultrasonography at 6 months after balloon angioplasty
- Secondary Outcome Measures
Name Time Method 1)Rutherford category at 12 months after balloon angioplasty 2)Restenosis with duplex ultrasonography at 12 months after balloon angioplasty