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Terminated Phase 3 Interventional Results available

A Study of Rivaroxaban to Reduce the Risk of Major Venous and Arterial Thrombotic Events, Hospitalization and Death in Medically Ill Outpatients With Acute, Symptomatic Coronavirus Disease 2019 (COVID-19) Infection

ClinicalTrials.gov ID: NCT04508023

Public ClinicalTrials.gov record NCT04508023. 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

A Multicenter, Randomized, Placebo-Controlled, Pragmatic Phase 3 Study Investigating the Efficacy and Safety of Rivaroxaban to Reduce the Risk of Major Venous and Arterial Thrombotic Events, Hospitalization and Death in Medically Ill Outpatients With Acute, Symptomatic COVID-19 Infection

Study identification

NCT ID
NCT04508023
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Janssen Research & Development, LLC
Industry
Enrollment
1,284 participants

Conditions and interventions

Interventions

  • Rivaroxaban Drug
  • Placebo Other
  • Standard of Care (SOC) Other

Drug · Other

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
Aug 12, 2020
Primary completion
May 31, 2022
Completion
May 31, 2022
Last update posted
Jul 17, 2023

2020 – 2022

United States locations

U.S. sites
17
U.S. states
14
U.S. cities
16
Facility City State ZIP Site status
University of Arizona Tucson Arizona 85721
Southern California Permanente Medical Group Los Angeles California 90027
Kaiser Permanente Northern California Oakland California 94612
University of Colorado Denver Aurora Colorado 80045
Florida Hospital Orlando Orlando Florida 32803
Emory University Atlanta Georgia 30308
Morehouse School of Medicine Atlanta Georgia 30310
Atlanta VA Medical Center Decatur Georgia 30033
Northshore Universite Healthsystem Evanston Illinois 60201
Meritus Center for Clinical Research Hagerstown Maryland 21742
Brigham & Women's Hospital Boston Massachusetts 02115
Henry Ford Hospital Detroit Michigan 48202
Mayo Clinic Rochester Minnesota 55905
Lenox Hill Hospital -Northwell Health New York New York 10075
Vanderbilt University Medical Center Nashville Tennessee 37235
Texas Health Physicians Group Fort Worth Texas 76107
Franciscan Research Center Tacoma Washington 98404

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04508023, 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 Jul 17, 2023 · Synced Jul 22, 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 NCT04508023 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →