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Prevention and Treatment of Hemodialysis Vascular Access Malfunction

Primary Purpose

End-Stage Renal Disease

Status
Withdrawn
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
angioplasty
surgery
Sponsored by
Vanderbilt University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for End-Stage Renal Disease focused on measuring End Stage Renal Disease, ESRD, Chronic Maintenance Hemodialysis

Eligibility Criteria

18 Years - 85 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Subjects with End Stage Renal Disease on chronic maintenance hemodialysis 3 times per week Have an arteriovenous (polytetrafluoroethylene) graft as vascular access Have a venous stenosis between 30% and 70% as determined by angiogram Exclusion Criteria: Native arteriovenous fistula Known previous vascular accesses complications, such as central vein stenosis, and multiple access surgeries >4 Unwilling to participate Allergy to iodine Absolute contraindication for surgery (e.g. medical condition precludes anesthesia and surgery) Known arterial limb stenosis or long vessel length venous stenosis which are unamenable to surgical or angioplasty techniques, respectively, and therefore prohibit randomization Known hypercoagulable state

Sites / Locations

  • Vanderbilt University Medical Center

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

No Intervention

Active Comparator

Active Comparator

Arm Label

1

2

3

Arm Description

control group

angioplasty intervention

surgery intervention

Outcomes

Primary Outcome Measures

To test the hypothesis that early intervention of a vascular access determined to be at increased risk of malfunction and thrombosis improves the long-term access outcome versus standard of care.

Secondary Outcome Measures

To determine which means of early intervention, surgery versus angioplasty, is medically and financially advantageous.

Full Information

First Posted
September 13, 2005
Last Updated
May 21, 2015
Sponsor
Vanderbilt University
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1. Study Identification

Unique Protocol Identification Number
NCT00179192
Brief Title
Prevention and Treatment of Hemodialysis Vascular Access Malfunction
Official Title
Prevention and Treatment of Hemodialysis Vascular Access Malfunction
Study Type
Interventional

2. Study Status

Record Verification Date
May 2015
Overall Recruitment Status
Withdrawn
Why Stopped
non-enrollment
Study Start Date
May 1998 (undefined)
Primary Completion Date
October 2006 (Actual)
Study Completion Date
October 2006 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Vanderbilt University

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Vascular access is considered the Achilles heel of the dialysis patient. It constitutes the largest single cause of morbidity in the chronic hemodialysis population, accounting for over 25% of hospitalizations at an estimated cost in the US of at least one billion dollars annually. Currently, complication free survival of vascular access ranges between 30-50% a year and multiple investigative efforts in this area have been initiated and are directed at prolonging the functional life of vascular accesses. It is not well established whether intervention prior to overt malfunction or thrombosis of the vascular access could reduce these complications and thereby improve the functional longevity of the access. Moreover, once accesses at potential risk are identified, it is not well established which method of intervention, Surgery vs. Angioplasty vs. Expectant Management, is superior in terms of clinical and financial outcome. The proposed study aims to determine whether early intervention of a vascular access determined to be at risk of malfunction and thrombosis improves the long term outcome and, specifically, which means of intervention is preferred.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
End-Stage Renal Disease
Keywords
End Stage Renal Disease, ESRD, Chronic Maintenance Hemodialysis

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
No Intervention
Arm Description
control group
Arm Title
2
Arm Type
Active Comparator
Arm Description
angioplasty intervention
Arm Title
3
Arm Type
Active Comparator
Arm Description
surgery intervention
Intervention Type
Procedure
Intervention Name(s)
angioplasty
Intervention Description
angioplasty performed at the time of the angiogram; approach and technique to be determined by the interventional radiologist
Intervention Type
Procedure
Intervention Name(s)
surgery
Intervention Description
surgical revision of patient's PTFE in a timely fashion not to exceed 72-96 hours after the angiogram; method of revision to be determined by the surgeon performing the procedure
Primary Outcome Measure Information:
Title
To test the hypothesis that early intervention of a vascular access determined to be at increased risk of malfunction and thrombosis improves the long-term access outcome versus standard of care.
Time Frame
2 years
Secondary Outcome Measure Information:
Title
To determine which means of early intervention, surgery versus angioplasty, is medically and financially advantageous.
Time Frame
2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Subjects with End Stage Renal Disease on chronic maintenance hemodialysis 3 times per week Have an arteriovenous (polytetrafluoroethylene) graft as vascular access Have a venous stenosis between 30% and 70% as determined by angiogram Exclusion Criteria: Native arteriovenous fistula Known previous vascular accesses complications, such as central vein stenosis, and multiple access surgeries >4 Unwilling to participate Allergy to iodine Absolute contraindication for surgery (e.g. medical condition precludes anesthesia and surgery) Known arterial limb stenosis or long vessel length venous stenosis which are unamenable to surgical or angioplasty techniques, respectively, and therefore prohibit randomization Known hypercoagulable state
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Talat A Ikizler, MD
Organizational Affiliation
Vanderbilt University Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Vanderbilt University Medical Center
City
Nashville
State/Province
Tennessee
ZIP/Postal Code
37232
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Prevention and Treatment of Hemodialysis Vascular Access Malfunction

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