MedPath

Special Drug Use Surveillance of LIXIANA Tablet- Long-term use in patients with venous thromboembolism

Phase 4
Conditions
Treatment and recurrence prevention of venous thromboembolism [VTE] (deep vein thrombosis [DVT] and pulmonary thromboembolism [PTE])
Registration Number
JPRN-UMIN000016387
Lead Sponsor
DAIICHI SANKYO COMPANY, LIMITED
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open public recruiting
Sex
All
Target Recruitment
1500
Inclusion Criteria

Patients who meet the following requirements when starting to receive LIXIANA (at the time of enrollment for [3]) will be considered for admission to the study:
[1] Patients who have just started to receive LIXIANA for the first time for the treatment and secondary (recurrence) prevention of VTE (DVT and PTE)
[2] Patients who are to start treatment with LIXIANA during the period of contract (as per the signed contract between the institution and the sponsor) and during the enrollment period
[3] Patients who have given written informed consent to the study

Exclusion Criteria

None

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
© Copyright 2025. All Rights Reserved by MedPath