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Completed Phase 3 Interventional Results available

Edoxaban vs. Warfarin in Subjects Undergoing Cardioversion of Nonvalvular Atrial Fibrillation (NVAF)

ClinicalTrials.gov ID: NCT02072434

Public ClinicalTrials.gov record NCT02072434. 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 May 11, 2026, 4:40 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, Open-Label Blinded Endpoint Evaluation (PROBE) Parallel Group Study Comparing Edoxaban (DU-176b) With Enoxaparin/Warfarin Followed by Warfarin Alone in Subjects Undergoing Planned Electrical Cardioversion of Nonvalvular Atrial Fibrillation

Study identification

NCT ID
NCT02072434
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Daiichi Sankyo
Industry
Enrollment
2,199 participants

Conditions and interventions

Interventions

  • Edoxaban Drug
  • Enoxaparin Drug
  • Warfarin Drug

Drug

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
Mar 24, 2014
Primary completion
Feb 2, 2016
Completion
Feb 2, 2016
Last update posted
Mar 14, 2019

2014 – 2016

United States locations

U.S. sites
28
U.S. states
13
U.S. cities
28
Facility City State ZIP Site status
Not listed Phoenix Arizona
Not listed Escondido California
Not listed Newport Beach California
Not listed Riverside California
Not listed San Francisco California
Not listed Santa Rosa California
Not listed Denver Colorado
Not listed Stamford Connecticut
Not listed Newark Delaware
Not listed Clearwater Florida
Not listed Daytona Beach Florida
Not listed Jupiter Florida
Not listed Rockledge Florida
Not listed Sarasota Florida
Not listed Tampa Florida
Not listed Boise Idaho
Not listed Auburn Maine
Not listed Rochester Minnesota
Not listed Allentown Pennsylvania
Not listed Butler Pennsylvania
Not listed Camp Hill Pennsylvania
Not listed Hershey Pennsylvania
Not listed Jackson Tennessee
Not listed Dallas Texas
Not listed Fort Worth Texas
Not listed Plano Texas
Not listed Tyler Texas
Not listed Richmond Virginia

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 200 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02072434, 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 Mar 14, 2019 · Synced May 11, 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 NCT02072434 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →