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The Boston Scientific ACCESS Trial (ACCESS)

Primary Purpose

Renal Disease, Kidney Failure

Status
Terminated
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
vascular access graft implantation
Sponsored by
Maquet Cardiovascular
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Renal Disease focused on measuring vascular access, hemodialysis

Eligibility Criteria

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

Inclusion Criteria: Need for early dialysis access (≤72 hours after implantation): Initiation of maintenance dialysis is recommended per K/DOQI or institutional guidelines; or Patient is currently receiving dialysis via catheter No prior implantation of synthetic graft in the arm to be treated Life expectancy of at least 2 years, based on physician's assessment of medical condition Exclusion Criteria: Patient younger than 18 years of age Any stenosis in the veins proximal to (downstream of) implant site, as determined previously or by current ultrasound Pregnancy Bleeding disorder, e.g., low platelet count (<50,000), hypercoagulable state, e.g., antithrombin III deficiency; antiphospholipid or anticardiolipin antibodies; Factor V Leiden; circulating Lupus anticoagulant; current, active heparin-induced thrombocytopenia; Protein C or S deficiency; or history of recurrent deep vein thrombosis not related to AV access. Active malignancy, e.g., condition either being treated or considered untreatable Active systemic infection, e.g., condition either being treated or considered untreatable Uncontrolled major symptomatic medical problem, e.g., undiagnosed severe pain, metabolic disturbance, fever, etc. Likelihood of poor compliance to required dialysis protocol, e.g., history of poor attendance to required clinic sessions or non-compliance to medication Mental incapacity; inability to understand treatment instructions Currently participating in another investigational drug or device study that clinically interferes with the endpoints of this study

Sites / Locations

  • Long Beach VA Medical Center
  • Saint Joseph's Hospital of Atlanta
  • Rush University Medical Center
  • Beth Israel Deaconess Medical Center
  • VA New Jersey Healthcare System
  • New York - Presbyterian, Columbia University Medical Center
  • Cleveland Clinic Foundation
  • University of Texas Southwestern / VA Medical Center

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Arm 1

Arm Description

Outcomes

Primary Outcome Measures

Secondary patency at 6 months as determined by ability of the graft to be used for vascular access for hemodialysis

Secondary Outcome Measures

Full Information

First Posted
November 30, 2005
Last Updated
June 26, 2012
Sponsor
Maquet Cardiovascular
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1. Study Identification

Unique Protocol Identification Number
NCT00260728
Brief Title
The Boston Scientific ACCESS Trial
Acronym
ACCESS
Official Title
ACCESS: Prospective, Multi-center Trial of the Fusion Vascular Access Graft for Patients Who Require Early Vascular Access for Hemodialysis
Study Type
Interventional

2. Study Status

Record Verification Date
June 2012
Overall Recruitment Status
Terminated
Study Start Date
December 2005 (undefined)
Primary Completion Date
May 2007 (Actual)
Study Completion Date
December 2008 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Maquet Cardiovascular

4. Oversight

5. Study Description

Brief Summary
The Boston Scientific ACCESS trial seeks to study the safety and to evaluate the success of the Fusion™ Vascular Access Graft for patients in need of early vascular access for hemodialysis.
Detailed Description
The Boston Scientific ACCESS trial seeks to study the safety and to evaluate the success of the Fusion™ Vascular Access Graft for patients in need of early vascular access for hemodialysis. The primary objective is to demonstrate that secondary patency at 6 months for the Fusion™ Vascular Access Graft is not less than an objective performance criterion (OPC) minus a clinically relevant margin (δ). The OPC represents secondary patency at 6 months for the standard of care access grafts. The secondary safety endpoint is the occurrence of CEC-adjudicated device or procedure related adverse events through 24 months post implant procedure, or through discharge for patients with unsuccessful device implantation. Secondary efficacy endpoints include:primary patency; primary assisted patency; ability to revise a failed graft; early access capability; time to hemostasis. Subjects will undergo a thorough medical assessment and physical examination pre-procedure and will be assessed peri-procedure. Enrolled subjects with a device implanted will be evaluated at 1, 6, 12, 18 and 24 months post implant procedure.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Renal Disease, Kidney Failure
Keywords
vascular access, hemodialysis

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
149 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Arm 1
Arm Type
Experimental
Intervention Type
Device
Intervention Name(s)
vascular access graft implantation
Intervention Description
vascular access graft implantation
Primary Outcome Measure Information:
Title
Secondary patency at 6 months as determined by ability of the graft to be used for vascular access for hemodialysis
Time Frame
6 Months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Need for early dialysis access (≤72 hours after implantation): Initiation of maintenance dialysis is recommended per K/DOQI or institutional guidelines; or Patient is currently receiving dialysis via catheter No prior implantation of synthetic graft in the arm to be treated Life expectancy of at least 2 years, based on physician's assessment of medical condition Exclusion Criteria: Patient younger than 18 years of age Any stenosis in the veins proximal to (downstream of) implant site, as determined previously or by current ultrasound Pregnancy Bleeding disorder, e.g., low platelet count (<50,000), hypercoagulable state, e.g., antithrombin III deficiency; antiphospholipid or anticardiolipin antibodies; Factor V Leiden; circulating Lupus anticoagulant; current, active heparin-induced thrombocytopenia; Protein C or S deficiency; or history of recurrent deep vein thrombosis not related to AV access. Active malignancy, e.g., condition either being treated or considered untreatable Active systemic infection, e.g., condition either being treated or considered untreatable Uncontrolled major symptomatic medical problem, e.g., undiagnosed severe pain, metabolic disturbance, fever, etc. Likelihood of poor compliance to required dialysis protocol, e.g., history of poor attendance to required clinic sessions or non-compliance to medication Mental incapacity; inability to understand treatment instructions Currently participating in another investigational drug or device study that clinically interferes with the endpoints of this study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Luis Sanchez, MD
Organizational Affiliation
Washington University School of Medicine, Barnes Jewish Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Long Beach VA Medical Center
City
Long Beach
State/Province
California
ZIP/Postal Code
90822
Country
United States
Facility Name
Saint Joseph's Hospital of Atlanta
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30342
Country
United States
Facility Name
Rush University Medical Center
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60612-3824
Country
United States
Facility Name
Beth Israel Deaconess Medical Center
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02215
Country
United States
Facility Name
VA New Jersey Healthcare System
City
East Orange
State/Province
New Jersey
ZIP/Postal Code
07018
Country
United States
Facility Name
New York - Presbyterian, Columbia University Medical Center
City
New York
State/Province
New York
ZIP/Postal Code
10032
Country
United States
Facility Name
Cleveland Clinic Foundation
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44195
Country
United States
Facility Name
University of Texas Southwestern / VA Medical Center
City
Dallas
State/Province
Texas
ZIP/Postal Code
75216
Country
United States

12. IPD Sharing Statement

Learn more about this trial

The Boston Scientific ACCESS Trial

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