Skip to content

Long-term Outcome After Edoxaban Versus Vitamin K Antagonists for Acute VTE

Long-term Outcome After Edoxaban Versus Vitamin K Antagonists for Acute VTE

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04007653
Acronym
HOKUSAIpostVTE
Enrollment
1200
Registered
2019-07-05
Start date
2017-04-25
Completion date
2020-12-31
Last updated
2019-07-05

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

Conditions

Chronic Thromboembolic Pulmonary Hypertension, Post Thrombotic Syndrome, Quality of Life, Venous Thromboembolic Disease

Keywords

Post thrombotic syndrome, Edoxaban, Vitamin K antagonist, Chronic Thromboembolic Pulmonary Hypertension, Quality of Life

Brief summary

The HOKUSAI post VTE study contains of two different research questions; one on the long term outcomes of deep vein thrombosis and one on the long term effects of pulmonary embolism, post thrombotic syndrome (PTS) and chronic thromboembolic pulmonary hypertension (CTEPH) respectively. Our aim of the study is to compare the long term outcomes along with the quality of life assessment of VTE in a group treated with heparin+VKA versus a group treated with heparin+edoxaban in the acute setting.

Interventions

OTHERObservation

No intervention

Sponsors

Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Participant in the HOKUSAI VTE trial

Exclusion criteria

* None

Design outcomes

Primary

MeasureTime frameDescription
Post thrombotic syndrome (PTS)up to 10 yearsPTS according to Villalta

Secondary

MeasureTime frameDescription
Chronic thromboembolic pulmonary hypertension (CTEPH)up to 10 yearsaccording to clinical and objective criteria

Countries

Netherlands

Contacts

Primary ContactIngrid Bistervels, MD
i.m.bistervels@amc.uva.nl+31205665976
Backup ContactRoisin Bavalia, MD
r.bavalia@amc.uva.nl0031 205667516

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 17, 2026