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Characterizing Recurrent Thromboembolism, Major Bleeding and All-Cause Death in Patients With Cancer-Associated Thromboembolism Treated With Rivaroxaban

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Bayer

Status

Completed

Conditions

Venous Thromboembolism

Treatments

Drug: Rivaroxaban (Xarelto, BAY59-7939)

Study type

Observational

Funder types

Industry

Identifiers

Details and patient eligibility

About

To estimate the real-world rates of recurrent Venous thromboembolism (VTE), major bleeding and all-cause mortality in patients with Cancer-associated thrombosis (CAT) treated with rivaroxaban

Enrollment

1,000 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adult patients (≥18 years-of-age) with active cancer
  • Patient with at least one index venous thromboembolism (VTE )
  • ≥6-months of continuous eligibility prior to the index VTE event (baseline period).
  • Newly initiated on rivaroxaban

Exclusion criteria

  • Patients with any medical claim for Deep vein thrombosis (DVT) or Pulmonary embolism (PE) during the 6 months pre-index date
  • Patients with prescription claim for anticoagulation therapy during the 6-month pre-index VTE period

Trial design

1,000 participants in 1 patient group

Cancer-associated thrombosis
Description:
Adult patients with active cancer with at least one index venous thromboembolism (VTE) and no anticoagulation use during the 6-months (baseline period) prior to the index VTE event
Treatment:
Drug: Rivaroxaban (Xarelto, BAY59-7939)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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