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Terminated Not applicable Interventional

A Multicenter Study to Evaluate the ROX Coupler in Subjects With Hypertension

ClinicalTrials.gov ID: NCT02895386

Public ClinicalTrials.gov record NCT02895386. 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 25, 2026, 12:36 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

A Prospective, Randomized, Adaptive, Double-Blind, Sham-Controlled, Multicenter Study to Evaluate the ROX Coupler in Subjects With Hypertension

Brief summary

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

To evaluate the safety and effectiveness of the ROX Coupler used to create an arteriovenous anastomosis in the iliac region (between the iliac artery and vein) in subjects with hypertension.

Study identification

NCT ID
NCT02895386
Recruitment status
Terminated
Study type
Interventional
Phase
Not applicable
Lead sponsor
ROX Medical, Inc.
Industry
Enrollment
30 participants

Conditions and interventions

Interventions

Device · Other

Eligibility (public fields only)

Age range
22 Years to 85 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
Mar 22, 2017 (Actual)
Primary completion
May 1, 2019 (Actual)
Completion
May 1, 2019 (Actual)
Last update posted
May 13, 2019

2017 – 2019

United States locations

U.S. sites
13
U.S. states
9
U.S. cities
12
Facility City State ZIP Site status
Cardiology P.C. Research Birmingham Alabama 35211 —
UAB Division of Cardiovascular Disease Birmingham Alabama 35294 —
The Cardiac and Vascular Institute Research Foundation Gainesville Florida 32605 —
Piedmont Heart Institute Atlanta Georgia 30309 —
Prairie Education and Research Cooperative Springfield Illinois 62769 —
Cardiology Associates Research Tupelo Mississippi 38801 —
Northwell Health - North Shore University Hospital Manhasset New York 11030 —
Northwell Health - Lenox Hill Hospital New York New York 10075 —
Duke University Hospital Durham North Carolina 27710 —
The Lindner Center for Research and Education at The Christ Hospital Cincinnati Ohio 45219 —
The MetroHealth System Cleveland Ohio 44109 —
OhioHealth Research Institute Columbus Ohio 43214 —
CAMC Clinical Trials Center Charleston West Virginia 25304 —

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 NCT02895386, 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 13, 2019 · Synced Oct 25, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02895386 live on ClinicalTrials.gov.

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