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Not listed Not applicable Interventional

Randomized Trial of COBRA PzF Stenting to Reduce Duration of Triple Therapy

ClinicalTrials.gov ID: NCT02594501

Public ClinicalTrials.gov record NCT02594501. 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 Jul 21, 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

COBRA PzF Stenting to Reduce the Duration of Triple Therapy in Patients Treated With Oral Anticoagulation Undergoing Percutaneous Coronary Intervention

Study identification

NCT ID
NCT02594501
Recruitment status
Not listed
Study type
Interventional
Phase
Not applicable
Lead sponsor
CeloNova BioSciences, Inc.
Industry
Enrollment
996 participants

Conditions and interventions

Interventions

  • COBRA PzF Device
  • Drug Eluting Stent Device

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
Feb 4, 2016
Primary completion
Apr 30, 2021
Completion
Oct 31, 2021
Last update posted
Oct 25, 2020

2016 – 2021

United States locations

U.S. sites
22
U.S. states
13
U.S. cities
21
Facility City State ZIP Site status
Christiana Care Health Services Newark Delaware 19718
University of Florida Jacksonville Florida 32209
Memorial Hospital Jacksonville Jacksonville Florida 32216
Sebastian River Medical Center Melbourne Florida 32901
Mt Sinai Medical Center Miami Beach Florida 33140
Augusta University Augusta Georgia 30912
University of Maryland St. Joseph Medical Center Towson Maryland 21204
Beth Israel Deaconess Medical Center Boston Massachusetts 02215
Minneapolis Heart Institute Minneapolis Minnesota 55407
Deborah Heart and Lung Center Browns Mills New Jersey 08015
Rutgers Robert Wood Johnson Medical Schoo New Brunswick New Jersey 08901
Northwell Health Manhasset New York 11030
NYU Winthrop Hospital Mineola New York 11501
North Ohio Heart Center Elyria Ohio 44035
Cleveland Clinic Fairview Park Ohio 44126
Mercy St. Vincent Medical Center Toledo Ohio 43608
Einstein Medical Center Philadelphia Pennsylvania 19141
Texas Cardiac Center Lubbock Texas 79410
Tyler Cardiovascular Consultants Tyler Texas 75701
Sentara Heart Hospital (Sentara Cardiovascular Research Institute) Norfolk Virginia 23507
Carilion Medical Center Roanoke Virginia 24014
Charleston Area Medical 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.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 26 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02594501, 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 Oct 25, 2020 · Synced Jul 21, 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 protocol, eligibility criteria, and contact information for NCT02594501 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →