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
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
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
NCT ID
NCT01001676
First Posted
October 26, 2009
Last Updated
November 14, 2014
Sponsor
University Health Network, Toronto
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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