CI

At a glance

ClinicalIndex Comparison Record
Phase 4Completed· 179 enrolled
Drug / intervention
Long DOAC +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04724460
NCT04724460Phase 4Completed

Optimal Duration of Anticoagulation Therapy for Low-risk Pulmonary Embolism Patients With Cancer

Takeshi Morimoto·interventional·Posted Jan 26, 2021·Updated Mar 11, 2025

In Brief

A Phase 4 clinical trial evaluating Long DOAC and Short DOAC for Venous Thrombosis and 2 related conditions. Completed, enrolled 179 participants across 1 site.

Detailed Summary

The primary purpose of this study is to determine the optimal duration of anticoagulation therapy (6 months versus 18 months) with direct oral anticoagulant (DOAC) for cancer-associated low-risk pulmonary embolism patients. The major secondary purpose of this study is to investigate whether home treatment of cancer-associated low-risk pulmonary embolism patients with rivaroxaban is feasible, effective, and safe through an observational management study.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesJapan
CollaboratorsBayer Yakuhin, Ltd.

Timeline

Phase 4CompletedFinished
202120222023202420252026
First PostedJan 26, 2021
Enrollment StartFeb 18, 2021
Primary CompletionSep 27, 2024
Study CompletionDec 31, 2024
TodayJul 2, 2026
Enrollment to primary: 3.6 yearsPosted 5.4 years ago

Interventions

Long DOACdrug

Administration of Rivaroxaban for 18 months

Short DOACdrug

Administration of Rivaroxaban for 6 months