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Completed Not applicable Interventional Results available

Clinical Evaluation of a Vascular Venous Anastomotic Connector [InterGraft VIG-only Study]

ClinicalTrials.gov ID: NCT02532621

Public ClinicalTrials.gov record NCT02532621. 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, 12:38 PM EDT

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

Official title

Clinical Evaluation of a Vascular Venous Anastomotic Connector for Minimally Invasive Connection of an Arteriovenous Graft for Hemodialysis [InterGraft VIG-only Study]

Brief summary

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

The InterGraft™ Venous Anastomotic Connector provides an endovascular, minimally invasive means for attachment of an arteriovenous graft to a vein in the upper extremity. The InterGraft™ Venous Anastomotic Connector facilitates creation of the arteriovenous graft connection to a vein in support of hemodialysis in subjects with End Stage Renal Disease. The InterGraft™ Venous Anastomotic Connector is used together with conventional suturing of the arterial anastomosis to facilitate creation of an arteriovenous graft in support of hemodialysis in subjects with End Stage Renal Disease.

Study identification

NCT ID
NCT02532621
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Phraxis, Inc.
Industry
Enrollment
158 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
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
Feb 21, 2018 (Actual)
Primary completion
Jan 19, 2022 (Actual)
Completion
Jan 19, 2022 (Actual)
Last update posted
Feb 6, 2025

2018 – 2022

United States locations

U.S. sites
10
U.S. states
6
U.S. cities
10
Facility City State ZIP Site status
Triad of Alabama/Flowers Hospital Dothan Alabama 36305 —
Cartersville Medical Center, LLC Cartersville Georgia 30120 —
Medical Center of Central Georgia - Navicent Health Macon Georgia 31201 —
Henry Ford Health System- Dept of Surgery Detroit Michigan 48202 —
Saint Louis University St Louis Missouri 63103 —
Surgical Specialists of Charlotte Charlotte North Carolina 28207 —
Medical University of South Carolina Charleston South Carolina 29425 —
McLeod Physician Associates II Florence South Carolina 29506 —
Regional Medical Center of Orangeburg and Calhoun Counties Orangeburg South Carolina 29118-1498 —
Spartanburg Regional Medical Center Spartanburg South Carolina 29303 —

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 NCT02532621, 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 Feb 6, 2025 · 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 NCT02532621 live on ClinicalTrials.gov.

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