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Completed Not applicable Interventional Results available

VasQ External Support for Arteriovenous Fistula

ClinicalTrials.gov ID: NCT03242343

Public ClinicalTrials.gov record NCT03242343. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 23, 2026, 12:55 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multi-center Prospective Study to Evaluate the Safety and Effectiveness of the VasQ External Support for Arteriovenous Fistula

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a prospective clinical study of the VasQ external support for arteriovenous fistulas. The device is designed to improve fistula outcomes by optimizing the geometrical configuration of the fistula, influencing hemodynamics, minimizing turbulence and promote laminar flow. All patients will be implanted with the VasQ device and will be followed up for a duration of 24 months.

Study identification

NCT ID
NCT03242343
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Laminate Medical Technologies
Industry
Enrollment
144 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 80 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 29, 2017 (Actual)
Primary completion
Oct 8, 2020 (Actual)
Completion
Apr 3, 2022 (Actual)
Last update posted
May 27, 2026

2017 – 2022

United States locations

U.S. sites
15
U.S. states
11
U.S. cities
14
Facility City State ZIP Site status
Grandview Medical Center Birmingham Alabama 35243 —
Arizona Kidney Disease & Hypertension Center Phoenix Arizona 85012 —
Saint Francis Medical Center Peoria Illinois 61637 —
Lutheran Medical Group/Indiana Ohio Heart Fort Wayne Indiana 46804 —
Brigham and Women's Hospital Boston Massachusetts 02115 —
Boston Medical Center Boston Massachusetts 02118 —
University of Michigan Ann Arbor Michigan 48109 —
Albany Medical College Albany New York 12208 —
Montefiore Medical Center New York New York 10467 —
Charlotte PA Charlotte North Carolina 28207 —
Duke University Medical Center Durham North Carolina 27710 —
Ohio State University Wexner Meidcal Center Columbus Ohio 43210 —
Greenville Health System Greenville South Carolina 29615 —
Cardiothoracic and Vascular Surgeons, P.A. Austin Texas 78756 —
Methodist DeBakey Heart and Vascular Center,The Methodist Hospital Houston Texas 77030 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03242343, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted May 27, 2026 · Synced Oct 23, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03242343 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →