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OpenTrials
Completed

NCT Number: NCT02063672

Lutonix® Drug Coated Balloon vs. Standard Balloon Angioplasty for Treatment of Femoropopliteal In-Stent Restenosis

To assess the safety and efficacy of the Lutonix Drug Coated Balloon for treatment of femoropopliteal artery (SFA) in-stent restenosis (ISR).

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Cardiology Associates, Fairhope, Alabama, United States

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Who can participate

Healthy volunteers accepted: No

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

Key Inclusion Criteria:

  • Male or non-pregnant female ≥18 years of age
  • Rutherford Clinical Category 2-4
  • Significant (≥ 50%) restenosis of a previous bare (not covered and not drug-eluting) nitinol stent(s) in the femoropopliteal artery
  • Lesion measures between 4 and 18 cm
  • Target vessel diameter between ≥4 and ≤6 mm and able to be treated with available device size matrix
  • A patent inflow artery free from significant lesion (≥50% stenosis) as confirmed by angiography
  • Successful crossing and predilatation of the target lesion with a guidewire
  • At least one patent native outflow artery to the ankle, free from significant (≥50%) stenosis as confirmed by angiography that has not previously been (nor planned to be) revascularized
  • No other prior vascular or surgical interventions within 2 weeks before and/or planned 30 days after the protocol treatment

Key Exclusion Criteria:

  • Life expectancy of <1 year
  • Patient is currently participating in an investigational drug or other device study or previously enrolled in this study NOTE: Enrollment in another drug or device clinical trial during the follow up period is not allowed
  • History of stroke within 3 months
  • History of MI, thrombolysis or angina within 2 weeks of enrollment
  • Prior vascular surgery of the index limb, with the exception of remote common femoral patch angioplasty separated by at least 2 cm from the target lesion
  • Target lesion involves a previously placed covered stent or drug-eluting stent
  • Grade 4 or 5 stent fracture (mal-aligned components or trans-axial spiral configuration) in the restenotic stent
  • Inability to take required study medications or allergy to contrast that cannot be adequately managed with pre- and post-procedure medication
  • Known inadequate distal outflow (>50 % stenosis of distal popliteal and/or all three tibial vessels), or planned future treatment of vascular disease distal to the target lesion
  • Intended use of adjunctive treatment modalities (i.e. laser, atherectomy, cryoplasty, scoring/cutting balloon, stents, etc.)

Treatment and study plan

Lutonix DCB

Device

Standard uncoated Balloon Angioplasty Catheter

Device

PTA Catheter

Primary outcomes

  1. Percentage of Participants With Primary Patency at 1 Year

    Time frame: 12 Months

    Primary patency is defined as freedom from clinically driven target lesion restenosis (TLR) and from Binary Restenosis.

  2. Percentage of Participants Without Primary Safety Events

    Time frame: 12 Months

    Primary Safety Events include: All Cause Perioperative (≤30 day) Death, Index Limb Amputation, Index Limb Reintervention and Index Limb Related Death at 1 Year

Secondary outcomes

  1. Percentage of Participants With Device Success

    Time frame: During the Index Procedure (90 mins)

    Device success is defined as, on a per device basis, the achievement of successful delivery and deployment of the study device(s) as intended at the intended target lesion, without balloon rupture or inflation/deflation abnormalities and a successful withdrawal of the study system.

  2. Percentage of Participants With Technical Success

    Time frame: During the Index Procedure (90 mins)

    Technical success of the balloon procedure is defined as the achievement of successful delivery and deployment of the study device(s) as intended at the intended target lesion and a successful withdrawal of the study system with the achievement of < 30% residual percent stenosis without deployment of a bail-out stent.

  3. Percentage of Participants With Procedural Success

    Time frame: During the Index Procedure (90 mins)

    Procedural Success is defined as attainment of ≤30% residual stenosis in the treatment area by independent core lab analysis without major adverse events (defined as occurrence of death, amputation of the target limb, or repeat revascularization of the target lesion) during the index procedure and through the hospital stay.

  4. Percentage of Participants With Primary Patency at 6 and 12 Months

    Time frame: 6 months and 12 months

    Primary Patency is defined as Freedom from CEC-adjudicated Clinically-Driven TLR and from Core laboratory-adjudicated Binary Restenosis. Binary restenosis is based on threshold Doppler peak systolic velocity ratio (PSVR) ≥ 2.5 (together with waveform analysis & color mosaic appearance) or based on angiographic ≥ 50% diameter stenosis (if angiography is performed although not required per protocol).

  5. Percentage of Participants With Secondary Patency at 6 Months and 12 Months

    Time frame: 6 months and 12 months

    Secondary patency is defined as the absence of Binary Restenosis as adjudicated by the blinded, independent core laboratory, independent of whether or not patency is re-established via an endovascular procedure.

  6. Percentage of Participants Without Clinically Driven Target Lesion Revascularization (TLR)

    Time frame: 6 months and 12 months

    Clinically-driven TLR is defined as revascularization of the target vessel with evidence of target vessel diameter stenosis >50% determined by duplex ultrasound or angiography and new distal ischemic signs (worsening ABI or worsening Rutherford Category associated with the target limb or due to clinical symptoms), OR revascularization of a target vessel with an in-lesion diameter stenosis of >70% by angiography, in the absence of the previously mentioned ischemic signs or symptoms.

  7. Percentage of Participants Without Target Lesion Revascularization (TLR)

    Time frame: 6 months and 12 months

    TLR is defined as any repeat revascularization procedure (percutaneous or surgical) of the original target lesion site.

  8. Percentage of Participants With Sustained Clinical Benefit Compared to Baseline

    Time frame: 6 months and 12 months

    Sustained clinical benefit is defined as an improvement in Rutherford Classification compared to baseline and freedom from target vessel revascularization. The Rutherford classification is a clinical means of describing peripheral artery disease along a seven-stage scale, with stage 0 representing asymptomatic presentation and stage 6 representing severe ischemic ulcers or frank gangrene. A decrease in units on the scale represents improvement in clinical symptoms.

  9. Change of Rutherford Classification From Baseline

    Time frame: 6 months and 12 months

    The Rutherford classification is a clinical means of describing peripheral artery disease along a seven-stage scale, with stage 0 representing asymptomatic presentation and stage 6 representing severe ischemic ulcers or frank gangrene. A decrease in units on the scale represents improvement in clinical symptoms.

  10. Change of Resting Ankle Brachial Index (ABI) From Baseline

    Time frame: 6 months and 12 months

    The ankle-brachial index (ABI) is the ratio of the blood pressure at the ankle to the blood pressure in the upper arm (brachium).

  11. Change in Walking Impairment Questionnaire From Baseline

    Time frame: 6 months and 12 months

    The Walking Impairment Questionnaire (WIQ) is a validated questionnaire that evaluates walking ability with a focus on walking distance, walking speed, and the ability to climb stairs. Participants answer each item on a Likert scale from 0 for "unable to do" to 4 for "no difficulty", and each response is weighted based on the difficulty of the task. The overall score is determined by dividing the weighted answers by the maximum possible weighted score and multiplying by 100. The overall score ranges from 0-100 with lower scores indicating lower performance.

  12. Change in Quality of Life From Baseline

    Time frame: 6 months and 12 Months

    EQ-5D is a standardized tool to assess patient-reported mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each dimension has 5 levels: no problems, or slight, moderate, severe, or extreme problems. Patients choose the appropriate level in each of the 5 dimensions, which results in a 1-digit number for each dimension. The digits for the 5 dimensions are converted into a single EQ-5D™ index score based on a set of population-based preference weights. For the U.S. general population, possible EQ-5D™ index scores range from -0.11 (i.e., 33333) to 1.0 (i.e., 11111) on a scale where 0.0 = death and 1.0 = perfect health. A downloadable scoring file is available at: https://www.ahrq.gov/rice/EQ5Dscore.htm.

    The EQ VAS records a patient's self-rated health on a vertical visual analogue scale, where the endpoints are labeled 'The best health you can imagine' (100) and 'The worst health you can imagine' (0). A higher VAS value indicates a higher quality of life.

  13. Percentage of Participants Without Major Vascular Complications (≤30 Day)

    Time frame: 30 Days

    Freedom from major vascular complications at 30 days follow-up

  14. Percentage of Participants Without All-Cause Death

    Time frame: 1 month, 6 months, and 12 months

    Mortality from any cause.

  15. Percentage of Participants Without Major Limb Amputation

    Time frame: 1 month, 6 months, and 12 months

    Major limb amputation is defined as amputation of the lower limb above the ankle.

  16. Percentage of Participants Without Minor Limb Amputation

    Time frame: 1 month, 6 months, and 12 months

    Minor limb amputation is defined as amputation of a part of the foot below the ankle.

  17. Percentage of Participants Without Target Vessel Revascularizations (TVR)

    Time frame: 1 month, 6 months, and 12 months

    A TVR is defined as a repeat revascularization procedure (percutaneous or surgical) of a lesion in the target vessel.

  18. Percentage of Participants Without Any Target Limb Reinterventions

    Time frame: 1 month, 6 months, and 12 months

    Any surgical intervention in the target limb.

Sponsors and collaborators

Lead sponsor

C. R. Bard

Industry

Registry information

Official study title

A Prospective, Multicenter, Single-Blind, Randomized, Controlled Trial Comparing the Lutonix® Drug Coated Balloon vs. Standard Balloon Angioplasty for Treatment of Femoropopliteal In-Stent Restenosis

Acronym: SFA ISR

Important dates

Study start
2014
Primary completion
2017
Study completion
2019
First posted
Feb 14, 2014
Registry last updated
Apr 11, 2019

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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