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Completed Phase 3 Interventional Results available

A Study Exploring Two Treatment Strategies in Patients With Atrial Fibrillation Who Undergo Catheter Ablation Therapy

ClinicalTrials.gov ID: NCT01729871

Public ClinicalTrials.gov record NCT01729871. 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 17, 2026, 9:33 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 Randomized, Open-label, Active-controlled Multi-center Study to Assess Safety of Uninterrupted Rivaroxaban vs. Usual Care in Subjects Undergoing Catheter Ablation Therapy for Atrial Fibrillation

Brief summary

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

The purpose of this exploratory study is to evaluate the safety of rivaroxaban and uninterrupted vitamin K antagonist (VKA) in adult participants with non-valvular atrial fibrillation (NVAF) who undergo catheter ablation as measured by post-procedure major bleeding events.

Study identification

NCT ID
NCT01729871
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Janssen Scientific Affairs, LLC
Industry
Enrollment
253 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
Feb 2013 (Type not available)
Primary completion
Oct 2014 (Actual)
Completion
Oct 2014 (Actual)
Last update posted
Mar 6, 2017

2013 – 2014

United States locations

U.S. sites
24
U.S. states
16
U.S. cities
24
Facility City State ZIP Site status
Not listed Beverly Hills California — —
Not listed Los Angeles California — —
Not listed Sacramento California — —
Not listed San Francisco California — —
Not listed Jacksonville Florida — —
Not listed Maywood Illinois — —
Not listed Kansas City Kansas — —
Not listed Boston Massachusetts — —
Not listed Saint Louis Park Minnesota — —
Not listed Ridgewood New Jersey — —
Not listed Flushing New York — —
Not listed Durham North Carolina — —
Not listed Columbus Ohio — —
Not listed Portland Oregon — —
Not listed Erie Pennsylvania — —
Not listed Hershey Pennsylvania — —
Not listed Philadelphia Pennsylvania — —
Not listed Nashville Tennessee — —
Not listed Austin Texas — —
Not listed Dallas Texas — —
Not listed Tyler Texas — —
Not listed Charlottesville Virginia — —
Not listed Seattle Washington — —
Not listed Tacoma Washington — —

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 20 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01729871, 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 6, 2017 · Synced Oct 17, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01729871 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →