Anticoagulation in Patients With Venous Thromboembolism and Cancer

NCT ID: NCT04618913

Last Updated: 2026-01-16

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

ACTIVE_NOT_RECRUITING

Total Enrollment

1 participants

Study Classification

OBSERVATIONAL

Study Start Date

2020-12-14

Study Completion Date

2026-04-06

Brief Summary

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This study is a retrospective analysis of observational cohorts using data from prospectively collected administrative/claims data to investigate treatment patterns,healthcare resource utilisation (HCRU), direct and indirect costs (where feasible), and safety and effectiveness outcomes in patients with VTE and active cancer or patients with VTE and history of cancer who initiate anticoagulant treatment with a VKA, LMWH or NOACs.

Detailed Description

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Conditions

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Neoplasms Embolism

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

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VTE and history of cancer

VTE and history of cancer

Apixaban

Intervention Type DRUG

Anticoagulant

Rivaroxaban

Intervention Type DRUG

Anticoagulant

Edoxaban

Intervention Type DRUG

Edoxaban

Dabigatran

Intervention Type DRUG

Dabigatran

VKA

Intervention Type DRUG

Vitamin K antagonist

LMWH

Intervention Type DRUG

Low Molecular Weight Heparin

VTE and active cancer

VTE and active cancer

Apixaban

Intervention Type DRUG

Anticoagulant

Rivaroxaban

Intervention Type DRUG

Anticoagulant

Edoxaban

Intervention Type DRUG

Edoxaban

Dabigatran

Intervention Type DRUG

Dabigatran

VKA

Intervention Type DRUG

Vitamin K antagonist

LMWH

Intervention Type DRUG

Low Molecular Weight Heparin

Interventions

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Apixaban

Anticoagulant

Intervention Type DRUG

Rivaroxaban

Anticoagulant

Intervention Type DRUG

Edoxaban

Edoxaban

Intervention Type DRUG

Dabigatran

Dabigatran

Intervention Type DRUG

VKA

Vitamin K antagonist

Intervention Type DRUG

LMWH

Low Molecular Weight Heparin

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* A VTE diagnosis
* Active cancer or history of cancer
* Treatment with VKA, NOAC (apixaban, rivaroxaban, dabigatran, edoxaban) or LMWH
* Age ≥ 18 years at the date of index VTE (Venous thromboembolic)

Exclusion Criteria

* Prior VTE diagnosis
* Diagnosis of prior atrial fibrillation
* Inferior Vena Cava (IVC) filter
* Prior exposure to (OAC) oral anticoagulation or (PAC)parenteral anticoagulation - note: Prophylactic use of (OAC)/(PAC) allowed.
* Pregnancy
* More than one (OAC) oral anticoagulation or (PAC) parenteral anticoagulation dispensed on the index date.
* Patients with less than one day of follow up
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Pfizer

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Pfizer CT.gov Call Center

Role: STUDY_DIRECTOR

Pfizer

Locations

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Pfizer Investigational Site

London, , United Kingdom

Site Status

Countries

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United Kingdom

Related Links

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https://pmiform.com/clinical-trial-info-request?StudyID=B0661150

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Other Identifiers

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B0661150

Identifier Type: -

Identifier Source: org_study_id

VICTORIE

Identifier Type: OTHER

Identifier Source: secondary_id

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