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Restenosis Following Paclitaxel Eluting Balloon Angioplasty of Hemodialysis Access Stenosis

Primary Purpose

Renal Failure

Status
Completed
Phase
Phase 2
Locations
Canada
Study Type
Interventional
Intervention
Percutaneous Transluminal Angioplasty (PTA)
Paclitaxel Eluting Balloon Angioplasty
Sponsored by
University Health Network, Toronto
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Renal Failure focused on measuring renal failure, Restenosis, Dialysis access, Paclitaxel, Angioplasty, Intimal hyperplasia

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Hemodialysis access located in the forearm or upper arm
  • Patient with clinical or hemodynamic evidence of graft dysfunction
  • Hemodialysis access is > 3 months old

Exclusion Criteria:

  • Intervention of the vascular access circuit within the past 30 days
  • Thrombosed/clotted access
  • Evidence of systemic infection or a local infection associated with the graft
  • Positive pregnancy test within 7 days before enrolment
  • Patient is scheduled for a kidney transplant

Sites / Locations

  • University Health Network

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Conventional Balloon Angioplasty

Drug Eluting Balloon Angioplasty

Arm Description

Outcomes

Primary Outcome Measures

Primary patency

Secondary Outcome Measures

Transonic blood flows

Full Information

First Posted
October 26, 2009
Last Updated
November 14, 2014
Sponsor
University Health Network, Toronto
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1. Study Identification

Unique Protocol Identification Number
NCT01001676
Brief Title
Restenosis Following Paclitaxel Eluting Balloon Angioplasty of Hemodialysis Access Stenosis
Official Title
Local Delivery of Paclitaxel for Prevention of Restenosis in Hemodialysis Access
Study Type
Interventional

2. Study Status

Record Verification Date
January 2012
Overall Recruitment Status
Completed
Study Start Date
February 2012 (undefined)
Primary Completion Date
July 2014 (Actual)
Study Completion Date
July 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Health Network, Toronto

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Introduction: Narrowing of the draining vein occurs in >50% of hemodialysis fistula and left untreated will lead to loss of access. The narrowing is due to excessive growth of tissue in the vessel wall (intimal hyperplasia). The standard treatment is balloon dilatation. However, narrowing will inevitably recur in 2-3 months hence requiring further dilatation. Intimal hyperplasia also occurs in the heart and leg circulation. The drug paclitaxel has been used with great success in preventing intimal hyperplasia in these vessels following balloon dilatation. Administer locally, paclitaxel inhibits excess tissue growth in the vessel wall. The investigators believe that this drug will have similar effect in hemodialysis access.. Objective: To assess the effect of paclitaxel in hemodialysis access with narrowing. Paclitaxel is delivered by a paclitaxel-coated balloon. This balloon dilates the narrow segment and simultaneously delivers paclitaxel to the vessel wall. Methodology: Patients with narrowed hemodialysis access are dilated with the paclitaxel-coated balloon or conventional balloon in randomized manner. The patency of the two groups are evaluated and compared at 6 months follow-up. Potential benefit: Decrease number of balloon dilatations and hence hospital admissions, improve dialysis fistula function, and decrease overall economic cost.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Renal Failure
Keywords
renal failure, Restenosis, Dialysis access, Paclitaxel, Angioplasty, Intimal hyperplasia

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
32 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Conventional Balloon Angioplasty
Arm Type
Active Comparator
Arm Title
Drug Eluting Balloon Angioplasty
Arm Type
Experimental
Intervention Type
Device
Intervention Name(s)
Percutaneous Transluminal Angioplasty (PTA)
Intervention Description
Angioplasty with the use of Conventional balloon
Intervention Type
Device
Intervention Name(s)
Paclitaxel Eluting Balloon Angioplasty
Other Intervention Name(s)
Passeo-18 Lux (Biotronik)
Intervention Description
Angioplasty with the use of paclitaxel eluting balloon
Primary Outcome Measure Information:
Title
Primary patency
Time Frame
at 6 months
Secondary Outcome Measure Information:
Title
Transonic blood flows
Time Frame
monthly for up to 6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Hemodialysis access located in the forearm or upper arm Patient with clinical or hemodynamic evidence of graft dysfunction Hemodialysis access is > 3 months old Exclusion Criteria: Intervention of the vascular access circuit within the past 30 days Thrombosed/clotted access Evidence of systemic infection or a local infection associated with the graft Positive pregnancy test within 7 days before enrolment Patient is scheduled for a kidney transplant
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kong Teng Tan, BCh MB
Organizational Affiliation
University Health Network, Toronto
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Health Network
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5G 2N2
Country
Canada

12. IPD Sharing Statement

Learn more about this trial

Restenosis Following Paclitaxel Eluting Balloon Angioplasty of Hemodialysis Access Stenosis

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