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Completed Phase 4 Interventional Results available

Study Of The Blood Thinner, Apixaban, For Patients Who Have An Abnormal Heart Rhythm (Atrial Fibrillation) And Expected To Have Treatment To Put Them Back Into A Normal Heart Rhythm (Cardioversion)

ClinicalTrials.gov ID: NCT02100228

Public ClinicalTrials.gov record NCT02100228. 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 Nov 5, 2026, 1:17 PM EST

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Official title

A Phase Iv Trial To Assess The Effectiveness Of Apixaban Compared With Usual Care Anticoagulation In Subjects With Non-valvular Atrial Fibrillation Undergoing Cardioversion

Brief summary

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

Some people can develop an abnormal heart beat known as "Atrial fibrillation" or "AF" that puts them at risk of developing clots in the heart. Those clots can travel in the blood circulation to the brain and cause a brain attack ("a stroke"). To prevent those clots forming, blood thinners (anti-coagulants) are used. Apixaban is a blood thinner that works by stopping one of the blood substances required for clotting ("Factor Xa"). It is approved and used to prevent clots forming in people with "AF". Other established blood thinners work by stopping clotting substances being made, known as "Vitamin K antagonists" or "VKAs". An example of this type is Warfarin (Coumadin). The good effects of all blood thinners are preventing clots, and they may also have bad effects of increasing the chance of bleeding. People with "AF", abnormal heart beat, may benefit from changing it back to a normal regular rhythm, known medically as "cardioversion". When this is done, people are currently most commonly treated with a "VKA" blood thinner (e.g. warfarin). The purpose of this study is to assess the good and bad effects ("efficacy" and "safety") of apixaban compared with warfarin in people with "AF" in whom an early cardioversion is planned.

Study identification

NCT ID
NCT02100228
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Pfizer
Industry
Enrollment
1,500 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
Jul 14, 2014 (Actual)
Primary completion
Feb 8, 2017 (Actual)
Completion
Feb 8, 2017 (Actual)
Last update posted
May 23, 2018

2014 – 2017

United States locations

U.S. sites
63
U.S. states
21
U.S. cities
35
Facility City State ZIP Site status
Brookwood Medical Center Birmingham Alabama 35209 —
Cardiovascular Associates of the Southeast, LLC Birmingham Alabama 35243 —
Integrated Medical Services, Inc./IMS Cardiology Avondale Arizona 85392 —
Chula Vista Cardiac Center Chula Vista California 91910 —
Hartford Hospital Hartford Connecticut 06102 —
Certified Physician Investigator Research Group LLC Altamonte Springs Florida 32714 —
Orlando Heart Specialists Altamonte Springs Florida 32714 —
The University of Chicago Medical Center Investigational Drug Service Pharmacy (office/storage) Chicago Illinois 60637 —
The University of Chicago Medical Center Investigational Drug Service Pharmacy Chicago Illinois 60637 —
University of Chicago Medical Center Chicago Illinois 60637 —
Chicago Medical Research, LLC Hazel Crest Illinois 60429 —
Franciscan Physician Network-Indiana Heart Physicians Indianapolis Indiana 46237 —
Franciscan St. Francis Health Indianapolis Indiana 46237 —
UK Good Samaritan Medical Office Building Lexington Kentucky 40508-2678 —
Good Samaritan Hospital Lexington Kentucky 40508-3008 —
University of Kentucky Medical Center Gill Heart Institute Lexington Kentucky 40536-0200 —
University of Kentucky Gill Heart Institute Lexington Kentucky 40536 —
University of Kentucky HealthCare/Albert. B, Chandler Hospital Lexington Kentucky 40536 —
Aim Clinic Louisville Kentucky 40202 —
Cardiology Outpatient Clinic Louisville Kentucky 40202 —
University of Louisville Clinical Trials Unit Louisville Kentucky 40202 —
University of Louisville Hospital Louisville Kentucky 40202 —
Robley Rex VA Medical Center Louisville Kentucky 40206 —
Alexandria Cardiology Clinic Alexandria Louisiana 71301 —
University of Massachusetts Worcester Research Pharmacy Worcester Massachusetts 01655 —
University of Massachusetts Worcester Worcester Massachusetts 01655 —
William Beaumont Hospital Royal Oak Michigan 48073 —
Abbott Northwestern Hopsital - Allina Health System Minneapolis Minnesota 55407 —
Minneapolis Heart Institute Foundation Minneapolis Minnesota 55407 —
University of Missouri Health Care System Columbia Missouri 65212 —
University of Missouri Health System, Investigational Drug Serivce Columbia Missouri 65212 —
University of Missouri Health System Columbia Missouri 65212 —
Saint Luke's Lipid and Diabetes Research Center Kansas City Missouri 64111 —
Mercy Hospital St. Louis St Louis Missouri 63141 —
Electrophysiology Associates Hackensack New Jersey 07601 —
Hackensack University Medical Center Hackensack New Jersey 07601 —
Robert Wood Johnson University Hospital New Brunswick New Jersey 08901 —
Rutgers Robert Wood Johnson Medical School Cardiovascular Institute New Brunswick New Jersey 08901 —
State University of New York (SUNY) Downstate Medical Center Brooklyn New York 11203 —
New York-Presbyterian/Queens Flushing New York 11355 —
Columbia University Medical Center/NY Presbyterian Hospital New York New York 10032 —
University of Cincinnati Medical Center Cincinnati Ohio 45219 —
ProMedica Physicians Cardiology Oregon Ohio 43616 —
ProMedica Toledo Hospital Toledo Ohio 43606 —
ProMedica Physicians Cardiology Toledo Ohio 43615 —
Hillcrest Medical Center Pharmacy Tulsa Oklahoma 74104 —
Oklahoma Heart Institute at Hillcrest Medical Center Tulsa Oklahoma 74104 —
Oklahoma Heart Institute Tulsa Oklahoma 74104 —
Cardiology Consultants of Philadelphia Bristol Pennsylvania 19007 —
Bryn Mawr Hospital Bryn Mawr Pennsylvania 19010 —
Bryn Mawr Medical Specialist Association Bryn Mawr Pennsylvania 19010 —
Penn State Hershey Medical Center Hershey Pennsylvania 17033 —
Pennsylvania Hospital Philadelphia Pennsylvania 19107 —
Einstein Healthcare Network Philadelphia Pennsylvania 19141 —
Cardiology consultants of Philadelphia Yardley Pennsylvania 19067 —
Baptist Hospital of Southeast Texas - Beaumont Beaumont Texas 77701 —
Southeast Texas Cardiology Associates II, L.L.P. Beaumont Texas 77702 —
Southeast Texas Cardiology Associates II, L.L.P Beaumont Texas 77702 —
Southeast Texas Clinical Research Center Beaumont Texas 77702 —
Utah Cardiology, PC Layton Utah 84041 —
Cardiovascular Associates of Virginia-Bon Secours St. Mary's Hospital Midlothian Virginia 23114 —
St. Francis Medical Center Midlothian Virginia 23114 —
Dominion Cardiovascular Specialists PLLC Richmond Virginia 23225 —

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 102 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02100228, 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 23, 2018 · Synced Nov 5, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02100228 live on ClinicalTrials.gov.

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