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UnknownNCT03951727

Stella Supera Siberia

Long Superficial Femoral Artery Stenting With SuperA Interwoven Nitinol Stents - Siberia

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
50 (estimated)
Sponsor
Meshalkin Research Institute of Pathology of Circulation · Network
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

Endovascular treatment with stenting is currently used in the treatment of femoro-popliteal lesions. This technique tends to extend to lesions for which the gold standard remains until now the open surgery treatment (lesions TASC C and D). The primary objective of the study was to evaluate the clinical efficacy at 12 months of the SuperA stent (Abbott) in the treatment of long de novo atherosclerotic lesions TASC C and D in patients with symptomatic peripheral arterial disease. The secondary objectives are to evaluate the clinical effectiveness of the SuperA stent at 24 months, according to clinical, morphological and haemodynamic criterias, the possible influence of calcifications and the quality of life of patients

Detailed description

Patient will be recruiting during 1 year. Patient will be followed in the study during 2 years. Pre-operative exams are collected. Patients are asked to give their oral authorization to participate in the study by their surgeon. Patient can be included up to the next day of the intervention. Endovascular treatment of femoropopliteal lesion with SuperA stents : Intervention will be achieved in operative room, under local anesthesia and sedation or general anesthesia. An angio-CT or an arteriography is necessary to attest the presence for TASC C or D lesion involving the superficial femoral and/or popliteal arteries. The long femoropopliteal lesion must be pre-dilated during 3 minutes with a balloon of 1mm diameter more than the stent to be implanted. A control arteriography will be done before the implantation of the stent and at the end of the intervention to assess the success of the procedure. If needed, endovascular treatment could be realized on the inflow or outflow in the same time. Patient follow-up : Patient follow-up is performed at 1, 6, 12 and 24 months. Follow-up will systematically include a clinical evaluation and a duplex scan with the ankle brachial index (ABI). The x-rays and the quality of life questionnaire will be done at 1, 12 and 24 months. All clinical surveillance events, complications and re-hospitalizations will be collected.

Conditions

Interventions

TypeNameDescription
DEVICEEndovascular treatment for PADLong femoropopliteal stenting with SuperA devices

Timeline

Start date
2019-05-13
Primary completion
2022-05-13
Completion
2022-05-13
First posted
2019-05-15
Last updated
2020-05-29

Locations

1 site across 1 country: Russia

Source: ClinicalTrials.gov record NCT03951727. Inclusion in this directory is not an endorsement.