Skip to main content
Clinical Trials/NCT02816398
NCT02816398
Completed
N/A

Vessel-Select Catheter System Feasibility Clinical Trial

Medtronic Endovascular0 sites26 target enrollmentJanuary 2014

Overview

Phase
N/A
Intervention
Not specified
Conditions
Renal Insufficiency, Chronic
Sponsor
Medtronic Endovascular
Enrollment
26
Primary Endpoint
Number of Participants With Sufficient Patency for Clinical Access
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

Feasibility clinical study to evaluate the safety and effectiveness of the catheter system for the percutaneous creation of an arteriovenous fistula for patients with end stage renal disease requiring dialysis access.

Registry
clinicaltrials.gov
Start Date
January 2014
End Date
January 2016
Last Updated
5 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Medtronic Endovascular
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients deemed medically eligible for AV fistula creation per institutional guidelines and/or clinical judgment
  • Patients diagnosed with chronic kidney disease classification stage IV or V
  • Adequate quality vein \>= 2 mm with confirmed clinically significant outflow based on pre-operative assessment
  • Adequate quality radial artery \>= 2 mm based on pre-operative assessment
  • Adequate collateral arterial perfusion
  • Radial artery-adjacent vein proximity \< = 1.5 mm
  • Able to provide informed consent
  • Able to travel to institution for follow up examination
  • Able to intraoperatively place an .014" guidewire in artery

Exclusion Criteria

  • Suspected skin disease
  • Immunocompromised patients (e.g. HIV positive)
  • Edema of extremities
  • Current diagnosis of carcinoma
  • Pregnancy or currently breast feeding
  • Diagnosed hypercoaguable state
  • Active infection
  • Evidence of vascular disease at target site
  • Pre-existing vascular disease that could confound study results
  • Vessel tortuosity or spasm preventing placement of .014" guidewire

Outcomes

Primary Outcomes

Number of Participants With Sufficient Patency for Clinical Access

Time Frame: 6 weeks

Arteriovenous fistula is patent as determined by auscultation or ultrasound and eligible for maturation assistance to achieve clinical access flow rate.

Number of Patients Achieving Dialysis Access

Time Frame: 6 weeks

Arteriovenous fistula is mature and patient has started dialysis using the fistula

Number of Patients on Dialysis Using the Arteriovenous Fistula or Has Adequate Access Flow Rate to Allow Dialysis

Time Frame: 3 months

Arteriovenous fistula is mature or has achieved a minimum clinically acceptable access flow rate as determined by doppler ultrasound assessment to support dialysis

Secondary Outcomes

  • Number of Patients Requiring Additional Interventions to Achieve Maturation and Dialysis Access(12 weeks)

Similar Trials