Atherosclerosis of the Peripheral Artery Clinical Trial
Official title:
Pilot Prospective Study of Two Methods of Revascularization of the Superficial Femoral Artery: Stenting in the Superficial Femoral Artery, and Stenting of the Superficial Femoral Artery, Supplemented by Fasciotomy in Hunter Channel in Patients With Steno-occlusive Lesions of Femoral-popliteal Segment TASC C, D
Comparison of two methods for revascularization of the superficial femoral artery: stenting of the superficial femoral artery vs. stenting of the superficial femoral artery supplemented with fasciotomy in Hunter canal in patients with steno-occlusive lesion of the femoro-popliteal segment of TASC C, D.
Status | Active, not recruiting |
Enrollment | 50 |
Est. completion date | November 2019 |
Est. primary completion date | October 2017 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 45 Years to 75 Years |
Eligibility |
Inclusion Criteria: - Patients with occlusive lesions of C and D type iliac segment, and with chronic lower limb ischemia (II-IV degree by Fontaine, 4-6 degree by Rutherford). - Patients who consented to participate in this study. Exclusion Criteria: - Chronic heart failure of III-IV functional class by NYHA classification. - Decompensated chronic "pulmonary" heart - Severe hepatic or renal failure (bilirubin> 35 mmol / l, glomerular filtration rate <60 mL / min); - Polyvalent drug allergy - Cancer in the terminal stage with a life expectancy less than 6 months; - Acute ischemic - Expressed aortic calcification tolerant to angioplasty - Patients with significant common femoral artery lesion - Patient refusal to participate or continue to participate in the study |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment
Country | Name | City | State |
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Russian Federation | NRICP | Novosibirsk |
Lead Sponsor | Collaborator |
---|---|
Meshalkin Research Institute of Pathology of Circulation |
Russian Federation,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Ankle-brachial index | Change in ankle-brachial index. | Baseline, 3 days after the operation, 6 month, 12 month, 2 years | No |
Primary | Ultrasound scan of the operated segment | The degree of stenosis in the operated segment. | Baseline, 3 days after the operation, 6 month, 12 month, 2 years | No |
Primary | CT-angiography of lower limb arteries | The degree of stenosis in the operated segment. CT-angiography of lower limb arteries at the control points will be done only if the detection of steno-occlusive lesions of the operated segment during the observation period, confirmed by ultrasound. | Baseline, 3 days after the operation, 6 month, 12 month, 2 years | No |
Secondary | Number of participants with a successful procedure of revascularization. | Number of participants with a successful procedure of revascularization. | During the operation. | No |
Secondary | Number of participants with complications during the operation. | Number of participants with complications during the operation. | During the operation. | No |
Secondary | Number of participants with limb salvage | Number of participants with limb salvage. | 3 days after the operation, 6 month, 12 month, 2 years | No |