MedPath

MARVEL-TTAS

Phase 4
Conditions
Deep vein thrombosis
Registration Number
JPRN-jRCTs071180059
Lead Sponsor
Tsujita Kenichi
Brief Summary

The purpose was to determine the appropriate effect of antithrombotic drugs using a new thrombogenicity assessment system (T-TAS) for pulmonary thromboembolism and deep vein thrombosis. However, the target number of cases was not reached, and analysis including the primary endpoint was difficult. The combination of the start of study enrollment and the outbreak of COVID-19 was a factor that made enrollment difficult.

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
20
Inclusion Criteria

New onset case of venous thromboembolism and deep vein thrombosis, who requires permanent antithrombotic therapy

Exclusion Criteria

1. contraindication of apixaban usage
2. Patients who are already taking antithrombotic or thrombolytic therapies
3. Patients who are judged as an inappropriate case to enroll

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Fluctuation of AR10-AU C30 value with or without bleeding events
Secondary Outcome Measures
NameTimeMethod
1) Fluctuation of AR10-AUC30 value in the case of venous thromboembolism<br><br>2) Fluctuation of AR10-AUC30 value after the remission venous thromboembolism<br><br>3) All death<br><br>4) Other adverse events
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