Study of the AFB and Stenting of the Iliac Arteries

Sponsor
Meshalkin Research Institute of Pathology of Circulation (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT02209350
Collaborator
(none)
202
1
2
100
2

Study Details

Study Description

Brief Summary

The aim of the study is to compare effectiveness and long-term results of aorta-femoral reconstructions and endovascular treatment in the patients with aorta-iliac lesions (TASC C,D).

Condition or Disease Intervention/Treatment Phase
  • Procedure: Aorta-femoral bypass
  • Procedure: Recanalization and stenting of aorta-iliac segment
  • Drug: Therapy: aspirin and clopidogrel
Phase 1

Study Design

Study Type:
Interventional
Actual Enrollment :
202 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Prospective Randomized Clinical Study of the Aorto-femoral Bypass and the Iliac Arteries With Stenting Recanalization Effectiveness in Patients With the Iliac Segment Occlusive Disease
Actual Study Start Date :
Aug 2, 2014
Anticipated Primary Completion Date :
Dec 1, 2022
Anticipated Study Completion Date :
Dec 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Group 1

Operations technique on the abdominal aorta. Aorta-femoral bypass. Medication: after surgery all patients are prescribed long-term aspirin (100 mg daily) and clopidogrel for 3 months (75 mg daily).

Procedure: Aorta-femoral bypass
Access to the femoral artery is performed through a lateral incision from the inguinal ligament. Operations technique on the abdominal aorta. Aorta-femoral bypass. Proximal anastomosis between the prosthesis and aorta is applied in the sort of "end-to-side" in the reconstruction by shunting. After jaws prosthesis conduction on hip distal anastomosis is formed with twisting controlling. In a case of preserved antegrade blood flow the femoral artery anastomosis applied in the sort of "end-to-side". If antegrade flow is absent, anastomosis is formed in the sort of "end to end".

Drug: Therapy: aspirin and clopidogrel
prescribed long-term aspirin (100 mg daily) and clopidogrel for 3 months (75 mg daily).

Active Comparator: Group 2

Standard endovascular treatment (stenting) in patients with the iliac segment occlusive disease. Medication: after stenting all patients are prescribed long-term aspirin (100 mg daily) and clopidogrel for 3 months (75 mg daily).

Procedure: Recanalization and stenting of aorta-iliac segment
Standard endovascular access is performed under local anesthesia and affected arterial segment is visualized. Stenosis or artery occlusion is passed with hydrophilic guide. In case of occlusion transluminal or subintimal (often "mixed") artery recanalization is performed. To maximize the preservation of the affected artery initial patency, occlusion recanalization is performed by ante-and retrograde accesses. Then stenosis or occlusion predilation is performed with balloon catheter (balloon catheter diameter is smaller than the affected artery diameter for 1-2 mm). After control angiography stent is installed in the aorta-iliac area throughout the lesion (lesion diameter corresponds to the stenotic arteries diameter).

Drug: Therapy: aspirin and clopidogrel
prescribed long-term aspirin (100 mg daily) and clopidogrel for 3 months (75 mg daily).

Outcome Measures

Primary Outcome Measures

  1. The primary composite endpoint (efficacy): primary patency, secondary patency [30 days]

    If a damage confirmed by duplex is detected, repeat intervention is performed on the side of the examined segment. The physiological parameter and questionnaire will be used.

  2. success of the procedure [30 days]

    Technical ability to perform the surgical intervention

  3. safeness: clinically significant bleeding, hematoma, infection of the prosthesis, infection of postoperative wound, lymphorrhea, renal failure, myocardial infarction, stroke, mortality, thrombosis of the operated segment, distal embolism [30 days]

    Identification of serious adverse events requiring correction of therapy or surgery. Will be used physiological parameter and questionnaire. Classification of bleeding will be used GUSTO (Severe or moderate)

Secondary Outcome Measures

  1. mortality in the long-term postoperative period [3 years]

  2. stroke in the remote postoperative period [3 years]

  3. myocardial infarction in the remote postoperative period [3 years]

  4. preservation of limb in the long-term postoperative period [3 years]

Eligibility Criteria

Criteria

Ages Eligible for Study:
45 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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), age: 47-75 years old.

  • 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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Novosibirsk Research Institute of Circulation Pathology Novosibirsk Russian Federation 630055

Sponsors and Collaborators

  • Meshalkin Research Institute of Pathology of Circulation

Investigators

  • Principal Investigator: Andrey Karpenko, MD, PhD, Novosibirsk Research Institute of Circulation Pathology

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Meshalkin Research Institute of Pathology of Circulation
ClinicalTrials.gov Identifier:
NCT02209350
Other Study ID Numbers:
  • TASC C,D
First Posted:
Aug 5, 2014
Last Update Posted:
May 29, 2020
Last Verified:
May 1, 2020
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 29, 2020