CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 26 enrolled
Drug / intervention
Percutaneous creation of an arteriovenous fistuladevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02816398
NCT02816398N/ACompleted

Vessel-Select Catheter System Feasibility Clinical Trial

Medtronic Endovascular·interventional·Posted Jun 28, 2016·Updated Feb 5, 2021

In Brief

A clinical study evaluating Percutaneous creation of an arteriovenous fistula for Renal Insufficiency, Chronic. Completed, enrolled 26 participants.

Detailed 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.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
Countries--

Timeline

N/ACompletedFinished
2014201520162017201820192020202120222023202420252026
First PostedJun 28, 2016
Enrollment StartJan 1, 2014
Primary CompletionOct 1, 2015
Study CompletionJan 1, 2016
TodayJul 2, 2026
Enrollment to primary: 1.8 yearsPosted 10.0 years ago

Interventions

Percutaneous creation of an arteriovenous fistuladevice

Use of catheter system for percutaneous creation of an arteriovenous fistula