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Trial record 1 of 3 for:    LUTONIX BTK
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Lutonix DCB Versus Standard Balloon Angioplasty for Treatment of Below-The-Knee (BTK) Arteries

This study is currently recruiting participants.
Verified October 2017 by C. R. Bard
Sponsor:
ClinicalTrials.gov Identifier:
NCT01870401
First Posted: June 6, 2013
Last Update Posted: October 13, 2017
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
Collaborator:
Bard Ltd
Information provided by (Responsible Party):
C. R. Bard
  Purpose
To assess the safety and efficacy of the Lutonix Drug Coated Balloon (DCB) for treatment of stenosis or occlusion of native below-the-knee arteries.

Condition Intervention
Critical Limb Ischemia Device: Lutonix DCB Device: Uncoated PTA Catheter

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single (Participant)
Primary Purpose: Treatment
Official Title: A Prospective, Multicenter, Single Blind, Randomized, Controlled Trial Comparing the Lutonix Drug Coated Balloon Versus Standard Balloon Angioplasty for Treatment of Below-the-Knee (BTK) Arteries(Lutonix BTK Trial)

Resource links provided by NLM:


Further study details as provided by C. R. Bard:

Primary Outcome Measures:
  • Freedom from BTK MALE+POD [ Time Frame: 30 days ]
    Composite of all-cause death, above-ankle amputation or major reintervention

  • Limb Salvage [ Time Frame: 6 months ]
    Freedom from the composite of above ankle amputation

  • Primary Patency [ Time Frame: 6 months ]
    Freedom from target vessel occlusion and clinically driven target lesion reintervention


Secondary Outcome Measures:
  • Wound healing [ Time Frame: 30 days; 6 months, 12 months, 24 months, and 36 months ]
    Healed or not, if not, improving, stagnant, worsening

  • Primary Patency [ Time Frame: 30 days and at 6 months, 12 months, 24 months, and 36 months ]
    Freedom from occlusion without clinically-driven Target Lesion Revascularization (TLR)

  • Hemodynamic outcome [ Time Frame: 30 days and at 6 months, 12 months, 24 months, and 36 months ]
    change in toe & ankle pressures

  • Clinically-driven TLR [ Time Frame: 30 days and at 6, 12, 24, and 36 months ]
    Revascularization performed on all randomized patients who returned with clinical symptoms, and if the subject has a target lesion diameter stenosis ≥ 50%.

  • Limb salvage in surviving subjects [ Time Frame: 30 days and at 6, 12, 24, and 36 months ]
    No Amputation of target limb


Estimated Enrollment: 1000
Study Start Date: May 2013
Estimated Study Completion Date: June 2020
Estimated Primary Completion Date: December 2017 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Lutonix DCB
Lutonix Paclitaxel Drug Coated Balloon
Device: Lutonix DCB
Other Name: LTX DCB
Active Comparator: PTA Catheter
Standard Uncoated PTA Catheter
Device: Uncoated PTA Catheter
Other Name: PTA

  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Male or non-pregnant female ≥18 years of age;
  • Rutherford Clinical Category 3, 4 & 5;
  • Life expectancy ≥ 1 year;
  • Significant stenosis (≥70%)
  • A patent inflow artery;
  • Target vessel(s) diameter between 2 and 4 mm;
  • Target vessel(s) reconstitute(s) at or above the ankle

Exclusion Criteria:

  • Pregnant or planning on becoming pregnant;
  • History of stroke within 3 months;
  • History of MI, thrombolysis or angina within 30 days of enrollment;
  • Planned major amputation (of either leg)
  • Prior major amputation if amputation occurred less than one year prior to enrollment and if patient is not independently ambulating;
  • GFR ≤ 30 ml/min per 1.73m2;
  • Acute limb ischemia;
  • In-stent restenosis of target lesion
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01870401


Contacts
Contact: Kimberly Kupcho kimberly.kupcho@crbard.com

  Show 64 Study Locations
Sponsors and Collaborators
C. R. Bard
Bard Ltd
Investigators
Principal Investigator: Patrick Geraghty, MD Washington University School of Medicine
Principal Investigator: Jihad Mustapha, MD Metro Health Hospital
Principal Investigator: Marianne Brodmann, MD Medical University Graz, Austria
  More Information

Responsible Party: C. R. Bard
ClinicalTrials.gov Identifier: NCT01870401     History of Changes
Other Study ID Numbers: CL0005-01
First Submitted: May 7, 2013
First Posted: June 6, 2013
Last Update Posted: October 13, 2017
Last Verified: October 2017

Additional relevant MeSH terms:
Ischemia
Pathologic Processes