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Effect of Direct Oral Anticoagulant (DOAC) in Adult Congenital Heart Disease Patients

Effect of Direct Oral Anticoagulant (DOAC) in Adult Congenital Heart Disease Patients - ACHD-DOAC

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000027808
Enrollment
600
Registered
2017-06-19
Start date
2017-06-12
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Adult congenital heart disease

Interventions

None listed

Sponsors

University of Tsukuba
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Prior registration or planned registration in the database called the Japanese Network of Cardiovascular Departments for Adult Congenital Heart Disease (JNCVD-ACHD), which was established by the Japanese Society for Adult Congenital Heart Disease 2) Age over 20 years old at the time of registration between 1/1/2011 and 31/6/2019 3) Treatment with one of the following anticoagulant drugs: warfarin, dabigatran, rivaroxaban, apixaban, or edoxaban

Exclusion criteria

Exclusion criteria: 1) Age less than 20 years old 2) Incapable of obtaining participant consent 3) Judged to be medically ineligible by the attending physician

Design outcomes

Primary

MeasureTime frame
Thromboembolic events and major bleeding events during administration

Secondary

MeasureTime frame
The following events during administration: 1) Minor bleeding events 2) Intracardiac thrombus 3) Other adverse events accompanying anticoagulant drug therapy 4) Changing (dose or type) or stopping anticoagulant drug therapy 5) Discontinuation of follow-up 6) Death 7) Hospitalization

Countries

Japan

Contacts

Public ContactTomoko Ishizu

University of Tsukuba Department of Cardiology, Faculty of Medicine

tomoco@md.tsukuba.ac.jp029-853-3143

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026