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Study to Gather Information How Often Venous Thromboembolism Occurs in Prostate Cancer Patients in Sweden and How This Condition is Treated With Blood Thinners

Prostate Cancer VTE in Sweden: Epidemiology and Anticoagulation Treatment of VTE

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03965741
Acronym
PRACTISE
Enrollment
97765
Registered
2019-05-29
Start date
2019-05-30
Completion date
2020-11-30
Last updated
2021-11-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Venous Thromboembolism (VTE)

Brief summary

Patients with cancer are at a significantly increased risk of experiencing a venous thromboembolism (VTE). VTE is defined by a blood clot in the leg or lower extremity (deep vein thrombosis) or a blood clot in the lung (pulmonary embolism) and is a leading cause of condition of being diseased and death among cancer patients. The goal of the study is to gather information how often venous thromboembolism (VTE) occurs in prostate cancer patients in Sweden and how this condition is treated with blood thinners.

Interventions

DRUGRivaroxaban (Xarelto, BAY59-7939)

Follow clinical administration

DRUGApixaban(Eliquis)

Follow clinical administration

Follow clinical administration

Sponsors

Janssen Research & Development, LLC
CollaboratorINDUSTRY
Bayer
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
MALE
Healthy volunteers
No

Inclusion criteria

* Initially all patients newly diagnosed with PCa between 2007-2016 with at least one year before the end of follow up date (31 December 2017) will be included. From this population, a sub-population of PCa patients with a first cancer-related VTE event will be selected.

Exclusion criteria

* None

Design outcomes

Primary

MeasureTime frameDescription
Incidence rates of post-VTE bleeding events leading to hospitalization, and mortality by anticoagulation treatmentRetrospective analysis between 2007 and 2016Among men with PCa and a first cancer-related VTE event
Duration of treatmentRetrospective analysis between 2007 and 2016Among men with PCa and a first cancer-related VTE event; To characterize the long-term anticoagulation treatment
Occurrence of recurrent VTE eventsRetrospective analysis between 2007 and 2016Among men with PCa and a first cancer-related VTE event; By long-term anticoagulation treatment (LMWH (Low molecular weight heparin), VKA (Vitamin K anticoagulants) or NOAC (Non-vitamin K oral anticoagulation)) and its estimated duration (up 3 months, 3-6 months, more than 6 months)
Time between a first cancer-related and a recurrent VTE eventRetrospective analysis between 2007 and 2016Among men with PCa and a first cancer-related VTE event
Subject's socio-demographic at the date of an incident PCa diagnosisRetrospective analysis between 2007 and 2016Among men with PCa
Subject's clinical characteristics at the date of an incident PCa diagnosisRetrospective analysis between 2007 and 2016Among men with PCa
Incidence rate of cancer-related VTERetrospective analysis between 2007 and 2016Among men with PCa
Cancer therapies in PCa at the initial time after diagnosisRetrospective analysis between 2007 and 2016Among men with PCa
Choice of drugRetrospective analysis between 2007 and 2016Among men with PCa and a first cancer-related VTE event; To characterize the long-term anticoagulation treatment

Secondary

MeasureTime frameDescription
Subject's clinical characteristics at the time of inclusion into the databaseRetrospective analysis between 2007 and 2016Among PCa-free men from the general population
Incidence rate of VTE eventsRetrospective analysis between 2007 and 2016Among PCa-free men from the general population
Subject's socio-demographic at the time of inclusion into the databaseRetrospective analysis between 2007 and 2016Among PCa-free men from the general population

Countries

Sweden

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026