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Clinical Trials/NCT02948166
NCT02948166
Unknown
Not Applicable

Prospective Randomized Clinical Trial of the Remote Endarterectomy and the Femoral Arteries Endovascular Treatments in Patients With the Femoral Artery Occlusive Disease (TASC C, D)

Meshalkin Research Institute of Pathology of Circulation1 site in 1 country174 target enrollmentJanuary 2016

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Steno-occlusive Desease of Femoro-popliteal Arterial Segment
Sponsor
Meshalkin Research Institute of Pathology of Circulation
Enrollment
174
Locations
1
Primary Endpoint
the change of lumen in target vessel
Last Updated
8 years ago

Overview

Brief Summary

Comparison of two methods for revascularization of the superficial femoral artery: remote endarterectomy vs. stenting of the superficial femoral artery cin patients with steno-occlusive lesion of the femoro-popliteal segment of TASC C, D

Detailed Description

Reported local percutaneous angioplasty and stenosis of femoral popliteal arteries indicate that the primary technical and clinical success above 95%. The technical success of recanalization of long occlusions femoral arteries less than 80%. Improvement of endovascular equipment designed for the treatment of total occlusions, increases the technical success of recanalization. The materials of the TASC II summarizes the results of several large studies that presented data on the operated segment artery patency at 56-73,7% within 2 years of observation. An alternative method of revascularization own femoral artery is remote endarterectomy. The two-year primary patency at remote endarterectomy is 86% (Moll F.L., Iio G.H. Closed superficial femoral artery endarterectomy: a 2-year follow up. Cardiovasc Surg. 1997; 5: 398-400). Primary assisted patency for 33 months 88% (Rosenthal D, Martin JD, Schubart PJ, Wellons ED. Remote. superficial femoral artery endarterectomy. J Cardiovasc Surg. (Torino) 2004; 45: 185-192). The length of the occlusion is not a limitation to the use of remote endarterectomy. Primary patency at 31 months was 60%.

Registry
clinicaltrials.gov
Start Date
January 2016
End Date
January 2019
Last Updated
8 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Meshalkin Research Institute of Pathology of Circulation
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients with occlusive lesions of C and D type femoral artery 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

Outcomes

Primary Outcomes

the change of lumen in target vessel

Time Frame: Baseline, 3 days after the operation, 6 month, 12 month, 2, 3 years

Secondary Outcomes

  • Number of participants with a successful procedure of revascularization.(During the operation.)
  • Number of participants with complications during the operation.(During the operation.)
  • Number of participants with limb salvage(Baseline, 3 days after the operation, 6 month, 12 month, 2, 3 years)

Study Sites (1)

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