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OpenTrials
Completed

NCT Number: NCT01816854

Endovascular Treatment of Atherosclerotic Lesions in the SFA Using the Sinus-superflex-635 Stent

In this prospective study, a newly developed self-expanding nitinol stent is evaluated for the treatment of atherosclerotic lesions in the superficial femoral artery and proximal popliteal artery.

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patient must sign informed consent prior to the index-procedure
  • Patient must be older than 18 years
  • Patient must be compliant with follow-up dates at 1 month and 12 months
  • Patients with intermittent claudication (Rutherford 2-3) and critical limb ischemia (Rutherford 4-5)
  • Target lesion is located in the superficial femoral artery (minimal 1 cm from origin of SFA and minimal 1 cm above the edge of the patella)
  • Reference vessel diameter ≥4.5 and ≤6.5 mm (visual estimate)
  • Patients with a TASC A, B or C lesion
  • Diameter stenosis of target lesion >50% or chronic occlusions
  • Inflow arteries are free of hemodynamically significant obstruction (i.e. ≥50%)
  • The popliteal artery (outflow) is free of hemodynamically significant obstruction (i.e. ≥50%)
  • At least 1 patent below-the-knee vessel (anterior tibial artery, posterior tibial artery or peroneal artery) till the ankle confirmed by baseline angiography

Exclusion criteria

  • Patients with Rutherford 1 and 6
  • Patiens with Serum creatinine > 2.0 mg/dL or renal dialysis
  • Patient takes esomeprazole or omeprazole
  • Patient is pregnant
  • Patient suffers from acute limb ischemia defined as any sudden decrease in limb perfusion causing a potential threat to limb viability
  • Target lesion cannot be crossed with a guidewire
  • Target lesion is located in the popliteal artery
  • Patients with a nickel-titanium allergy
  • Patients with an aneurysm in the superficial femoral artery and popliteal artery
  • Patients with a TASC D lesion
  • Patients with a life expectancy <1 year
  • Patients with scheduled elective non-vascular procedures within 3 months after index-procedure, vascular procedures are allowed within 3 months after index-procedure if it is guaranteed that acetylic salicylic acid and clopidogrel intake is not interrupted
  • Patients with previous bypass surgery in the SFA
  • Patients with intolerance to antithrombotic medication (acetylic salicylic acid, clopidogrel, ticlopidine, glycoprotein IIb/IIIa inhibitors, direct thrombin inhibitors, etc)
  • Patient has not been premedicated with acetylic salicylic acid (at least 80 mg/day) 2 hours before the index-procedure
  • Patient has not been premedicated with clopidogrel (600 mg/day) 2 hours before the index-procedure

Treatment and study plan

Stenting

Device

Primary outcomes

  1. Binary restenosis

    Time frame: 12 months

    Binary restenosis is defined as a re-obstruction ≥ 50% of the target lesion (peak systolic velocity ratio > 2.4).

Secondary outcomes

  1. Immediate procedural outcome (procedural, technical and device success)

    Time frame: peri-procedural

    Procedural success: combination of technical success, device success and absence of procedural complications.

    Technical success: successful vascular access and completion of the endovascular procedure and immediate morphological success with less than 30% residual diameter reduction of the treated lesion on completion angiography.

    Device success: exact deployment of the device according to the instructions for use as documented with suitable imaging modalities and in case of digital substraction angiography, in at least two different imaging projections.

  2. Distribution of Rutherford stages

    Time frame: 12 months

  3. Primary sustained clinical improvement

    Time frame: 12 months

    Defined as sustained upward shift of at least one category on the Rutherford classification without the need for repeated target lesion revascularization (TLR) in surviving patients.

  4. Secondary sustained clinical improvement at 12 months

    Time frame: 12 months

    Defined as sustained upward shift of at least one category on the Rutherford classification including the need for repeated TLR in surviving patients.

  5. Mortality

    Time frame: 30-day mortality

    post-procedural

  6. Mortality

    Time frame: 12 months

  7. Repeated target lesion revascularization (TLR) rate

    Time frame: 12 months

  8. Repeated target extremity revascularization (TER) rate

    Time frame: 12 months

  9. Amputation rate

    Time frame: 12 months

  10. Rate of patient clopidogrel resistance

    Time frame: 1 month

Sponsors and collaborators

Lead sponsor

be Medical

Industry

Registry information

Important dates

Study start
2012
Primary completion
2017
Study completion
2017
First posted
Mar 22, 2013
Registry last updated
Dec 20, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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