IN.PACT™ AV Access IDE Study

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Medtronic

Status

Completed

Conditions

Arteriovenous Fistula Occlusion
Fistula
Arteriovenous Fistula Stenosis
Arteriovenous Fistula

Treatments

Device: Standard Balloon Angioplasty
Device: IN.PACT AV DCB

Study type

Interventional

Funder types

Industry

Identifiers

NCT03041467
APV-IN.PACT AV Access

Details and patient eligibility

About

To evaluate the safety and efficacy of the IN.PACT™ AV Access Drug Coated Balloon (DCB) compared to percutaneous transluminal angioplasty (PTA) for treatment of subjects presenting with de novo or non-stented restenotic obstructive lesion of native arteriovenous dialysis fistulae (AVF) in the upper extremity.

Full description

This is a prospective, global, multi-center, single-blinded, 1:1 randomized clinical trial evaluating the IN.PACT™ AV Access Drug Coated Balloon (DCB) compared to percutaneous transluminal angioplasty (PTA) for treatment of subjects presenting with de novo or non-stented restenotic obstructive lesion of native arteriovenous dialysis fistulae (AVF) in the upper extremity. The trial will be conducted in up to 30 sites in the United States, Japan, and New Zealand.

Enrollment

330 patients

Sex

All

Ages

21+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patient is ≥21 years of age.
  • Patient has a life expectancy of ≥ 12 months
  • Patient has a native AV fistula created ≥ 60 days prior to the index procedure
  • The target AV fistula has undergone successful dialysis for at least 8 of 12 sessions during a four week period
  • Patient has a de novo and/or non-stented restenotic lesion located between the arteriovenous anastomosis and axillosubclavian junction with ≥50% stenosis. Note: If the lesion is located in the anastomosis, the treatment may be delivered up to 2 cm upstream on the arterial side. If the lesion is located in the cephalic arch, the treatment may be delivered up to 2 cm into the subclavian vein
  • Patient has a target lesion or a tandem lesion that is ≤ 100 mm in length (by visual estimate) Note: Tandem lesions may be enrolled provided they meet all of the following criteria: Separated by a gap of ≤ 30mm (3 cm), total combined lesion length, including 30 mm gap, ≤ 100 mm, and able to be treated as a single lesion
  • Patient has a target vessel diameter of 4.0 - 12.0 mm (by visual estimate).
  • Patient underwent successful crossing of the target lesion with the guide wire and pre-dilatation with a high pressure PTA balloon defined as: residual stenosis of ≤ 30% and absence of a flow limiting dissection (Grade ≥ C) or perforation
  • Patient provides written consent prior to enrollment in the study
  • Patient is willing to comply with all follow-up evaluations at specified times

Exclusion criteria

  • Women who are breastfeeding, pregnant, or are intending to become pregnant, or men intending to father children
  • Patient is receiving immunosuppressive therapy
  • Patient is anticipating a kidney transplant within 6 months of enrollment into the study
  • Patient has undergone prior intervention of access site within 30 days of index procedure
  • Patient with anticipated conversion to peritoneal dialysis
  • Patient has an infected AV access or systemic infection
  • Patient has planned surgical revision of access site
  • Patient with secondary non-target lesion requiring treatment within 30-days post index procedure
  • Patient with hemodynamically significant central venous stenoses that cannot be successfully treated prior to treatment of the target lesion
  • Patient with target AVF or access circuit which previously had or currently has a thrombosis
  • Patients judged to have a lesion that prevents complete inflation of an angioplasty balloon or proper placement of the delivery system
  • Patient with target lesion located central to the axillosubclavian junction
  • Patient has significant arterial inflow lesion requiring treatment more than 2 cm upstream from the anastomosis in the AV access
  • Patient has presence of pseudoaneurysm or aneurysm requiring treatment at the lesion site
  • Patient has presence of a stent located in the target AV access circuit
  • Patients with known allergies or sensitivities to paclitaxel
  • Patient with known contraindication, including allergic reaction, or sensitivity to contrast material that cannot be adequately pre-treated
  • Patient who cannot receive recommended antiplatelet and/or anticoagulant therapy
  • Patient with clinically significant Steal Syndrome requiring treatment
  • Patient is enrolled in another investigational drug, device, or biological study and has not completed the primary endpoint, or was previously enrolled in this study
  • Patient has a comorbid-condition that, in the judgment of the Investigator, may cause him/her to be non-compliant with the protocol of confound data interpretation

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

330 participants in 2 patient groups

IN.PACT AV DCB
Experimental group
Description:
PTA will be performed using the IN.PACT AV Access Drug Coated Balloon. IN.PACT AV Access DCB was the device name used during the clinical study. Medtronic has changed the name of the device to IN.PACT™ AV Paclitaxel-Coated Balloon Catheter (also referred as IN.PACT AV DCB). Hence, throughout posting, the study device will be referred to as the "IN.PACT AV DCB."
Treatment:
Device: IN.PACT AV DCB
Standard Balloon Angioplasty
Active Comparator group
Description:
PTA will be performed using a commercially available uncoated PTA balloon.
Treatment:
Device: Standard Balloon Angioplasty

Trial documents
2

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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