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Completed Not applicable Interventional Results available

Medtronic Resolute Onyx 2.0 mm Clinical Study

ClinicalTrials.gov ID: NCT02412501

Public ClinicalTrials.gov record NCT02412501. 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 Sep 5, 2026, 3:39 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 Clinical Evaluation of the Medtronic Resolute Onyx Zotarolimus-Eluting 2.0 mm Stent Resolute Onyx 2.0 mm Clinical Study

Brief summary

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

The purpose of this trial is to assess the safety and efficacy of the Resolute Onyx Zotarolimus-Eluting Coronary Stent System for the treatment of de novo lesions in native coronary arteries that allows the use of a 2.0 mm diameter stent.

Study identification

NCT ID
NCT02412501
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Medtronic Vascular
Industry
Enrollment
101 participants

Conditions and interventions

Interventions

Device

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
Apr 5, 2015
Primary completion
Feb 12, 2017
Completion
Feb 20, 2019
Last update posted
Jul 1, 2019

2015 – 2019

United States locations

U.S. sites
17
U.S. states
13
U.S. cities
16
Facility City State ZIP Site status
Scripps Green Hospital La Jolla California 92037
Morton Plant Hospital Clearwater Florida 33756
Saint John's Hospital Springfield Illinois 62701
St. Vincent Heart Center of Indiana Indianapolis Indiana 46290
Barnes Jewish University St Louis Missouri 63110
NYU Langone Medical Center New York New York 10016
The Mount Sinai Medical Center New York New York 10029
Saint Francis Hospital Roslyn New York 11576
Duke University Medical Center Durham North Carolina 27705
Sanford Medical Center Fargo North Dakota 58102
University Hospitals Elyria Medical Center Elyria Ohio 44035
Geisinger Medical Center Danville Pennsylvania 17822
Lankenau Medical Center Wynnewood Pennsylvania 19096
AnMed Health Medical Center Anderson South Carolina 29621
Centennial Medical Center Nashville Tennessee 37205
Dallas VA Medical Center Dallas Texas 75216
East Texas Medical Center Tyler Texas 75701

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 NCT02412501, 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 1, 2019 · Synced Sep 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02412501 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →