Use and Safety of the LUTONIX® Drug Coated Balloon Catheter in Arteries of the Lower Extremity

Terminated

• Conditions: Peripheral Artery Disease
• Interventions: Device: Lutonix Drug Coated Balloon Catheter

• Registration Number: NCT02043951
• Lead Sponsor: C. R. Bard

Brief Summary

The registry will enroll patients with claudication or critical limb ischemia and angiographically significant lesion(s) in arteries of the lower extremity. Subjects will be treated with the Lutonix® Drug Coated Balloon Catheter for approved indications according to the current country-specific Instructions for Use (IFU) and followed clinically for 1 year.

Detailed Description

This post-market registry is intended to assess the clinical use and safety of the Lutonix® Drug Coated Balloon Catheter in a heterogeneous patient population in real world clinical practice. Up to 500 patients will be enrolled in order to allow identification and assessment of rare adverse events (AEs) as well as outcomes in subpopulations defined by subject and lesion characteristics. All subjects will be followed for 1 year.

This registry is performed with marketed devices within the indications for use. There are no additional treatments or exams that will take place within this registry.

Study Timeline

• Study Start: 2014-01
• Study First Submitted: 2014-01-17
• Study First Submitted QC: 2014-01-21
• Study First Posted: 2014-01-23
• Primary Completion: 2015-12
• Study Completion: 2016-01
• Status Verified: 2016-07
• Last Update Submitted: 2016-07-12
• Last Update Posted: 2016-07-13

Recruitment & Eligibility

• Status: TERMINATED
• Sex: All
• Target Recruitment: 59

Inclusion Criteria

1. ≥ 18 years of age;
2. Rutherford Clinical Category ≤ 5;
3. Patient or Legally Authorized Representative is willing to provide informed consent and comply with the required follow up;
4. Stenotic or obstructive vascular lesions in artery(s) of the lower extremity;
5. Lesion(s) can be treated with available LUTONIX Drug Coated Balloon Catheter device size matrix per current country-specific IFU.

Exclusion Criteria

1. Patient is currently participating in an active phase of another investigational drug or device study;
2. Inability to take recommended medications as stated in the IFU or non-controllable allergy to contrast.

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
Single Arm: Lutonix Drug Coated Balloon	Lutonix Drug Coated Balloon Catheter	-

Primary Outcome Measures

Name	Time	Method
Efficacy: Freedom from target lesion revascularization (TLR)	12 months
Safety	30 Days	Freedom from the composite endpoint of target vessel revascularization (TVR), major amputation and major reintervention (new bypass graft, jump/interposition graft revision, or thrombectomy/thrombolysis) of index limb and device- and procedure-related death.

Secondary Outcome Measures

Name	Time	Method
Procedural Success	30 days, 6 and 12 months	Attainment of ≤30% residual stenosis by visual estimate in the treatment area above the knee and attainment of ≤50% residual stenosis by visual estimate in the treatment area below the knee without major adverse events during the index procedure.
Freedom separately from each of the following adverse events listed below:	30 days, 6 and 12 months	* All-cause death; * Device- and procedure-related mortality; * Unexpected device or drug-related AEs; * Index limb amputation (major and minor reported separately); * Reintervention for treatment of thrombosis of the target vessel; * Reintervention for embolization to its distal vasculature; * TLR (at 6 months); * TVR; * Composite of all-cause perioperative (≤30 day) death and from the following: index limb amputation, index limb reintervention, and index-limb-related death; * Major amputation and major reintervention (new bypass graft, jump/interposition graft revision, or thrombectomy/thrombolysis) of index limb.
Acute Device Success	30 days, 6 and 12 months	Device success is defined as, a per device basis, the achievement of successful delivery and deployment of the registry device(s) as intended at the intended target lesion, without balloon rupture or inflation/deflation abnormalities and a successful withdrawal of the registry system. If a device is inserted into the subject but not used due to user error (e.g. inappropriate balloon length or transit time too long) this device will not be included in the device success assessment.

Trial Locations

Locations (8)

The Vein Institute of Toronto; 🇨🇦 Toronto, Ontario, Canada

Christchurch Hospital; 🇳🇿 Christchurch, New Zealand

Wellington Regional Vascular Centre; 🇳🇿 Newtown, Wellington, New Zealand

Tauranga Hospital; 🇳🇿 Tauranga, New Zealand

Hospital Kuala Lumpur; 🇲🇾 Kuala Lumpur, Malaysia

Hospital Universiti Kebangsaan; 🇲🇾 Kuala Lumpur, Malaysia

Hospital Universiti Sains Malaysia; 🇲🇾 Kubang Kerian Kelantan, Malaysia

Hospital Umum Sarawak; 🇲🇾 Sarawak, Malaysia