Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 3 Interventional Results available

A Study of PRT-201 Administered Immediately After Radiocephalic Arteriovenous Fistula(AVF) Creation in Patients With Chronic Kidney Disease (CKD) (PATENCY-1)

ClinicalTrials.gov ID: NCT02110901

Public ClinicalTrials.gov record NCT02110901. 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 19, 2026, 3:34 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

Multicenter, Double-Blind, Placebo-Controlled Study of PRT-201 Administered Immediately After Radiocephalic Arteriovenous Fistula Creation in Patients With Chronic Kidney Disease

Brief summary

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

This research study is designed to assess the safety and effectiveness of an experimental drug called PRT-201 in patients both receiving or expecting to receive dialysis who have chronic kidney disease and who are undergoing surgery to create a new access point to their bloodstream for hemodialysis. PRT-201 is a protein that has been shown in previous research studies to help keep vessels patent when applied to the outside surface of the blood vessels (arteries and veins) in patients who undergo surgery to create an arteriovenous fistula (AVF). The purpose of this study is to determine whether PRT-201 when applied to a limited segment of your blood vessel (about 2 inches) immediately after surgery is safe and improves the patency of your AVF.

Study identification

NCT ID
NCT02110901
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Proteon Therapeutics
Industry
Enrollment
349 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 100 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
Jul 2014 (Actual)
Primary completion
Dec 2016 (Actual)
Completion
Dec 2018 (Actual)
Last update posted
Jul 9, 2019

2014 – 2018

United States locations

U.S. sites
35
U.S. states
18
U.S. cities
32
Facility City State ZIP Site status
University of Alabama at Birmingham Birmingham Alabama 35294 —
AKDHC Medical Research Services , LLC Phoenix Arizona 85012 —
AKDHC Medical Research Services, LLc Tucson Arizona 85719 —
Alliance Research Center Laguna Hills California 92653 —
VA Medical Center Long Beach Long Beach California 90822 —
Keck University Hospital at USC Los Angeles California 90033 —
Kaiser Permanente Medical Center San Diego California 92120 —
California Institute of Renal Research San Diego California 92123 —
UCSF Division of Vascular & Endovascular Surgery San Francisco California 94143 —
Rush Medical Center Chicago Illinois 60612 —
Renal Care Associates Peoria Illinois 61603 —
Lutheran Hospital Network of Indiana Fort Wayne Indiana 46804 —
University of Iowa Hospitals and Clinics Iowa City Iowa 52242 —
University of Louisville Louisville Kentucky 40202 —
Tulane University New Orleans Louisiana 70112 —
Louisiana State University Health Sciences Center Shreveport Louisiana 71130 —
Maine Medical Center Portland Maine 04102 —
University of Maryland Baltimore Maryland 21201 —
University of Maryland Shore Medical Center at Easton Easton Maryland 21601 —
Beth Israel Deaconess Medical Center Boston Massachusetts 02215 —
Brigham and Women's Hospital Boston Massachusetts 02482 —
University of Massachusetts Medical Center Worcester Massachusetts 01655 —
Mount Sinai Medical Center New York New York 10029 —
University of North Carolina at Chapel Hill Chapel Hill North Carolina 27599 —
Duke University Durham North Carolina 27710 —
W.G. Hefner VA Medical Center Salisbury North Carolina 28144 —
Wake Forest Winston-Salem North Carolina 27157 —
University of Cincinnati Medical Center Cincinnati Ohio 45267 —
University of Cincinnati Cincinnati Ohio 45267 —
Ohio State University Columbus Ohio 43210 —
The University of Oklahoma College of Medicine Tulsa Oklahoma 74104 —
Lehigh Valley Health Network Allentown Pennsylvania 18103 —
VA Pittsburg Healthcare System Pittsburgh Pennsylvania 15240 —
The Methodist Hospital Houston Texas 77030 —
Lake Washington Vascular Center Bellevue Washington 98004 —

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 NCT02110901, 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 Jul 9, 2019 · Synced Oct 19, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02110901 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →