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NCT02558465: JPMS-XAR-VTE

Special Drug Use Investigation of Xarelto for Venous Thromboembolism (VTE)

Completed Last updated 1 November 2022
What this trial tests

trial testing Rivaroxaban (Xarelto, BAY59-7939) in Venous Thromboembolism in 2,540 participants. Completed in 31 May 2021.

Timeline
13 November 2015
Primary endpoint
1 April 2021
31 May 2021

Quick facts

Lead sponsorBayer
StatusCompleted
Study typeOBSERVATIONAL
Enrollment2,540
Start date13 November 2015
Primary completion1 April 2021
Estimated completion31 May 2021
Sites1 location across Japan

Drugs / interventions tested

Conditions studied

Sponsor

Bayer — full company profile →

Who can join

Eligibility, any sex, with Venous Thromboembolism. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The objective of this investigation is to assess safety and effectiveness of Xarelto under practice routine use in VTE secondary prevention after acute DVT, focusing on hemorrhagic-related AEs, recurrent venous thromboembolism (PE/DVT), all-cause mortality. This study is a company sponsored, one- arm prospective cohort study with patients to whom Rivaroxaban treatment for VTE (PE/DVT) has been chosen. The study includes a standard observation period (1 year) and an extension survey period (2 years, at the longest).

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of Rivaroxaban (Xarelto, BAY59-7939)

Trials testing the same drug.

Other recruiting trials for Venous Thromboembolism

Currently open trials in the same condition.

Other Bayer trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT02558465.

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