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Completed Phase 3 Interventional Results available

A Study of Rivaroxaban (JNJ-39039039) on the Venous Thromboembolic Risk in Post-Hospital Discharge Patients

ClinicalTrials.gov ID: NCT02111564

Public ClinicalTrials.gov record NCT02111564. 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 22, 2026, 3:17 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

Medically Ill Patient Assessment of Rivaroxaban Versus Placebo in Reducing Post-Discharge Venous Thrombo-Embolism Risk

Study identification

NCT ID
NCT02111564
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Janssen Research & Development, LLC
Industry
Enrollment
12,024 participants

Conditions and interventions

Interventions

  • Rivaroxaban, 10 mg Drug
  • Rivaroxaban, 7.5 mg Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
40 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
Jan 6, 2014
Primary completion
Mar 5, 2018
Completion
May 2, 2018
Last update posted
Nov 24, 2019

2014 – 2018

United States locations

U.S. sites
135
U.S. states
39
U.S. cities
135
Facility City State ZIP Site status
Not listed Birmingham Alabama
Not listed Mobile Alabama
Not listed Sheffield Alabama
Not listed Scottsdale Arizona
Not listed Fort Smith Arkansas
Not listed Little Rock Arkansas
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Not listed Atlantis Florida
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Not listed Albuquerque New Mexico
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Not listed Cortlandt Manor New York
Not listed Jamaica New York
Not listed Johnson City New York
Not listed Manhasset New York
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Not listed Staten Island New York
Not listed Valhalla New York
Not listed Durham North Carolina
Not listed Greensboro North Carolina
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Not listed Canton Ohio
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Not listed Pawtucket Rhode Island
Not listed Columbia South Carolina
Not listed Summerville South Carolina
Not listed Athens Tennessee
Not listed Amarillo Texas
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Not listed Channelview Texas
Not listed Corsicana Texas
Not listed Dallas Texas
Not listed Fort Worth Texas
Not listed Houston Texas
Not listed McAllen Texas
Not listed Tyler Texas
Not listed Norfolk Virginia
Not listed Richmond Virginia
Not listed Roanoke Virginia
Not listed Richland Washington
Not listed Seattle Washington
Not listed Huntington West Virginia
Not listed La Crosse Wisconsin
Not listed Marshfield Wisconsin

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 459 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02111564, 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 Nov 24, 2019 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02111564 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →