ASSESS Study: Evaluation of ABSOLUTE™ Stent System for Occluded Arteries

Abbott

Status and phase: Completed; Phase 4

Conditions: Peripheral Vascular Diseases

Treatments: Device: ABSOLUTE™: Self-Expandable Peripheral Nitinol Stent

Study type: Interventional

Funder types: Industry

Identifiers

NCT00180505

04-100

Details and patient eligibility

About

The purpose of this study is to investigate the performance of the ABSOLUTE™ .035 peripheral self-expanding stent system in preventing restenosis of occluded or stenotic superficial femoral or proximal popliteal arteries.

Full description

The treatment of stenosis in superficial femoral arteries and/or proximal popliteal arteries with stenting is associated with high restenosis rates, especially with the first generation stents (stainless steel). Currently, self-expandable nitinol stents are commercialized which lead to higher primary patency rates as compared to the first generation stents, even in longer lesions. However, until now most data available are retrospective and uni-center. The ASSESS study is a prospective multi-center study investigating the performance (restenosis rate, patency rates) of the ABSOLUTE™. 035 peripheral self-expandable stent in longer lesions (lesion length from 4.00 mm to 200.00 mm).

Moreover, literature shows stent fracture in nitinol stents, with a possible clinical relationship. For this reason, the ASSESS study will analyze the stent fractures of the ABSOLUTE™ stent, and a possible relationship between stent fracture and restenosis.

Enrollment: 120 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• De novo lesion of the superficial femoral artery (SFA) or proximal popliteal artery within the following parameters:

  • 10 mm distal to the origin of the profunda femoris (= 10 mm from the femoral bifurcation in the SFA) and
  • 20 mm from the proximal margin of the intercondylar fossa.

• Patients must have symptomatic leg ischemia, requiring treatment of the superficial femoral/proximal popliteal vessel

• Target vessel reference diameter visually estimated to be > 4.0 mm and < 7.0 mm

• Target lesion length visually estimated to be > 40 mm and < 200 mm

• If the patient has a contralateral SFA or contralateral proximal popliteal lesion, this lesion can be treated as a non-target lesion. The time and way of treatment of the non-target lesion will be left up to the discretion of the investigator

• At least one-vessel run-off to the foot confirmed by baseline angiography

• Patent common iliac artery, common femoral artery and profunda confirmed by baseline angiography. The patent common iliac artery can be obtained during the index procedure by a successful treatment prior to the treatment of the target lesion. Successful treatment being defined as attainment of final residual diameter stenosis of < 30% without death, stroke, bleeding requiring > 2 units transfusion, or any other complication which was device or procedure related.

• Patient is acceptable candidate for femoral-popliteal artery bypass surgery

Exclusion criteria

• Previous ipsilateral femoro-popliteal or femoro-tibial surgery
• Presence of a stent in the target vessel
• Prescheduled staged procedures of multiple lesions within the ipsilateral iliac or ipsilateral popliteal arteries within 30 days after the index procedure
• Co-existing aneurysmal disease of the abdominal aorta or iliac or popliteal arteries
• Acute thrombophlebitis or deep vein thrombus
• Any immunosuppressive disorders, groin infection, or acute systemic infection due to any cause or any viral or bacterial infection
• Significant gastrointestinal (GI) bleed within the past month that would contraindicate the use of anti-platelet therapy
• Hemodynamic instability
• Target lesion is restenotic from previous intervention

Trial design

Primary purpose: Treatment

Allocation: Non-Randomized

Interventional model: Single Group Assignment

Masking: None (Open label)

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120 participants in 1 patient group

1

Other group

Description:

The purpose of the ASSESS Registry is to investigate the performance of the ABSOLUTE™ .035 Peripheral Self-Expanding Stent System (ABSOLUTE™ Stent) in preventing restenosis of occluded or stenotic superficial femoral or proximal popliteal arteries.

Treatment:

Device: ABSOLUTE™: Self-Expandable Peripheral Nitinol Stent