An Observational Study to Learn More About How Safe Treatment With Rivaroxaban is in Children in Japan With Venous Thromboembolism

NCT06278051 | Completed

• 1 other identifier: 21411
• Study Type: observational
• Target: 320
• Locations: 1 country
• Sites: 2

Brief Summary

This is an observational study in which only data will be collected from children with venous thromboembolism who are prescribed rivaroxaban or warfarin by their doctors. Venous thromboembolism (VTE) is a condition in which people have problems due to the formation of blood clots in their veins. The study drug rivaroxaban is an approved treatment for VTE in children and adults in Japan. It is a blood thinner that prevents the blood from clotting by blocking a protein responsible for blood clotting. Warfarin is another blood thinner that is available for VTE. In this study warfarin is the reference drug. A previous study was carried out to learn about how well rivaroxaban works and how safe it is in children with VTE. However, to better understand the safety of this drug in children, more knowledge is needed about the use of rivaroxaban in the real world. The main purpose of this study is to learn more about the occurrence of major bleeding in children taking rivaroxaban. Major bleeding can be bleeding within the skull, bleeding inside the eye, bleeding from an organ in the digestive system, or bleeding which requires being given blood from a donor. In addition, this study will help learn more about the following in children with VTE:

• The occurrence of major bleeding during treatment with rivaroxaban and during treatment with warfarin
• The occurrence of bleeding of importance in children being treated with rivaroxaban and in children being treated with warfarin. Bleeding of importance in children can be: bleeding from the lung, blood in the kidney, heavy menstrual bleeding
• The occurrence of major bleeding and bleeding of importance in children who are taking drugs called anti platelet agents and NSAIDs to prevent blood clots at the same time as rivaroxaban, who are taking a drug that blocks the action of a protein called 'CYP3A4' at the same time as rivaroxaban, who have reduced kidney function, who have taken rivaroxaban for a long time, or who have taken other drugs by mouth to prevent blood clots before starting rivaroxaban
• The occurrence of repeated VTE on treatment with rivaroxaban and on treatment with warfarin The children with VTE in this study are already receiving rivaroxaban or warfarin treatment as part of their regular care from their doctors. The data will come from an electronic health records database created by a company called Medical Data Vision. The data will be collected between January 2021 and June 2024. Researchers will look at the health information from children less than 18 years of age with VTE in Japan who are prescribed treatment with rivaroxaban or warfarin during the study period. In this study, only available data from routine care are collected. No visits or tests are required as part of this study

Conditions

Venous Thromboembolism

Outcome Measures

Primary Outcomes (2)

• Incidence of major bleeding in participants treated with rivaroxaban

  Major bleeding is defined as composite of composite of intracranial hemorrhage, intraocular bleeding, upper gastrointestinal bleeding, lower gastrointestinal bleeding, bleeding requiring for blood transfusion

  Retrospective analysis from January 2021 to June 2024

• Clinical characteristics and demographics of participants with pediatric VTE treated with rivaroxaban

  Characteristics and demographics of participants will include e.g., age and gender, diagnosis and prior treatment, past medical history, concomitant diseases, and concomitant medication. They will be described.

  Retrospective analysis from January 2021 to June 2024

Secondary Outcomes (3)

• Incidence of major bleeding in participants treated with warfarin

  Retrospective analysis from 01 January 2021 to 30 June 2024

• Incidence of bleeding important in pediatrics in participants treated with rivaroxaban and treated with warfarin as reference

  Retrospective analysis from 01 January 2021 to 30 June 2024

• Incidence of major bleeding and bleeding important in pediatrics in participants treated with rivaroxaban and in special target patient groups

  Retrospective analysis from 01 January 2021 to 30 June 2024

Study Arms (2)

Xarelto (Rivaroxaban, BAY59-7939)

Drug: Rivaroxaban granules for oral suspension

Warfarin

Drug: Warfarin

Interventions

Rivaroxaban granules for oral suspension DRUG

Treatment dose and period decided by its prescription

Also known as: Xarelto, BAY59-7939

Xarelto (Rivaroxaban, BAY59-7939)

Warfarin DRUG

Treatment dose and period decided by its prescription

Warfarin

Eligibility Criteria

• Age: 0 Months - 18 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Child (0-17), Adult (18-64)
• Sampling Method: Non-Probability Sample

Study Population

Patients with pediatric VTE treated with rivaroxaban or warfarin in real-world clinical practice in Japan between 01 January 2021 and 30 June 2024

You may qualify if:

• Age less than 18 years
• Diagnosis of VTE at any point before and including the index date
• Receiving a prescription/dispensation of rivaroxaban or warfarin

You may not qualify if:

• none

Sponsors & Collaborators

• Bayer: lead
• Janssen Pharmaceutical Companies (formerly Johnson & Johnson Pharmaceutical Research & Development L.L.C.): collaborator

Study Sites (2)

Many facilities

Multiple Locations, Japan

Location

Bayer

Osaka, 530-0001, Japan

Location

MeSH Terms

Conditions

Venous Thromboembolism

Interventions

Suspensions; Rivaroxaban; Warfarin

Condition Hierarchy (Ancestors)

Thromboembolism; Embolism and Thrombosis; Vascular Diseases; Cardiovascular Diseases

Intervention Hierarchy (Ancestors)

Colloids; Complex Mixtures; Dosage Forms; Pharmaceutical Preparations; Thiophenes; Sulfur Compounds; Organic Chemicals; Morpholines; Oxazines; Heterocyclic Compounds, 1-Ring; Heterocyclic Compounds; 4-Hydroxycoumarins; Coumarins; Benzopyrans; Pyrans; Heterocyclic Compounds, 2-Ring; Heterocyclic Compounds, Fused-Ring

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: RETROSPECTIVE
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: February 19, 2024
• First Posted: February 26, 2024
• Study Start: February 19, 2024
• Primary Completion: November 11, 2024
• Study Completion: November 11, 2024
• Last Updated: May 12, 2026

Record last verified: 2026-05

Data Sharing

• IPD Sharing: Will not share

Locations

JP (2)