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Completed Phase 4 Interventional Results available

A Study of Rivaroxaban for Early Discharge of Low Risk Pulmonary Embolism From the Emergency Department

ClinicalTrials.gov ID: NCT02584660

Public ClinicalTrials.gov record NCT02584660. 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 26, 2026, 4:51 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

MulticEnter Trial of Rivaroxaban for Early disCharge of pUlmonaRY Embolism From the Emergency Department

Brief summary

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

The purpose of the study is to evaluate that low risk Pulmonary Embolism (PE) participants who are discharged from the Emergency Department (ED) to the home environment and treated with rivaroxaban as outpatients have fewer total days in the hospital for bleeding and/or venous thromboembolism (VTE) events through Day 30 compared to participants who are treated with initial hospitalization and standard-of-care.

Study identification

NCT ID
NCT02584660
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Janssen Scientific Affairs, LLC
Industry
Enrollment
114 participants

Conditions and interventions

Interventions

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
Oct 15, 2015 (Actual)
Primary completion
Mar 22, 2017 (Actual)
Completion
Mar 22, 2017 (Actual)
Last update posted
Jun 1, 2018

2015 – 2017

United States locations

U.S. sites
50
U.S. states
22
U.S. cities
50
Facility City State ZIP Site status
Not listed Montgomery Alabama — —
Not listed Chandler Arizona — —
Not listed Phoenix Arizona — —
Not listed Tucson Arizona — —
Not listed Los Angeles California — —
Not listed Sacramento California — —
Not listed Sylmar California — —
Not listed New Haven Connecticut — —
Not listed Washington D.C. District of Columbia — —
Not listed Pensacola Florida — —
Not listed Tampa Florida — —
Not listed Davenport Iowa — —
Not listed Iowa City Iowa — —
Not listed Baltimore Maryland — —
Not listed Springfield Massachusetts — —
Not listed Detroit Michigan — —
Not listed Jackson Michigan — —
Not listed Lansing Michigan — —
Not listed Royal Oak Michigan — —
Not listed St Louis Missouri — —
Not listed Atlantic City New Jersey — —
Not listed Camden New Jersey — —
Not listed Brooklyn New York — —
Not listed Buffalo New York — —
Not listed New York New York — —
Not listed Stony Brook New York — —
Not listed Chapel Hill North Carolina — —
Not listed Charlotte North Carolina — —
Not listed Durham North Carolina — —
Not listed Winston-Salem North Carolina — —
Not listed Cincinnati Ohio — —
Not listed Cleveland Ohio — —
Not listed Toledo Ohio — —
Not listed Zanesville Ohio — —
Not listed Portland Oregon — —
Not listed Allentown Pennsylvania — —
Not listed Bethlehem Pennsylvania — —
Not listed Philadelphia Pennsylvania — —
Not listed Pittsburgh Pennsylvania — —
Not listed West Reading Pennsylvania — —
Not listed Charleston South Carolina — —
Not listed Dallas Texas — —
Not listed Fort Worth Texas — —
Not listed Houston Texas — —
Not listed Salt Lake City Utah — —
Not listed Charlottesville Virginia — —
Not listed Bellingham Washington — —
Not listed Everett Washington — —
Not listed Spokane 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.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02584660, 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 Jun 1, 2018 · Synced Oct 26, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02584660 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →