Clinical Trials Directory

Trials / Terminated

TerminatedNCT00260728

The Boston Scientific ACCESS Trial

ACCESS: Prospective, Multi-center Trial of the Fusion Vascular Access Graft for Patients Who Require Early Vascular Access for Hemodialysis

Status
Terminated
Phase
Phase 2 / Phase 3
Study type
Interventional
Enrollment
149 (actual)
Sponsor
Maquet Cardiovascular · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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.

Conditions

Interventions

TypeNameDescription
DEVICEvascular access graft implantationvascular access graft implantation

Timeline

Start date
2005-12-01
Primary completion
2007-05-01
Completion
2008-12-01
First posted
2005-12-02
Last updated
2012-06-27

Locations

8 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT00260728. Inclusion in this directory is not an endorsement.