Keio interhospital Cardiovascular Studies - Atrial Fibrillation Registry

Keio interhospital Cardiovascular Studies - Atrial Fibrillation Registry - KiCS AF Registry

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000022229

Enrollment

3333

Registered

2016-05-08

Start date

2012-09-20

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

Atrial Fibrillation, Stroke

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: All patients with diagnosis of atrial fibrillation patients (diagnosed or referred within 6 months).

Exclusion criteria

Exclusion criteria: 1. Patients who were not able to give consent 2. Younger than 20 years old 3. Patients who are considered inappropriate to participate in the study by the treating physician.

Design outcomes

Primary

Measure	Time frame
1. Death (all-cause death, cardiovascular death, non-cardiovascular death) 2. Stroke (ischemic, hemorrhagic, unknown) 3. Systemic embolism 4. Major bleeding, non-major bleeding with specific healthcare provider responses 5. Major adverse cardiovascular event (acute myocardial infarction, unstable angina, undergoing percutaneous coronary intervention, heart failure)	—

Secondary

Measure	Time frame
Quality-of-life measured by the Atrial Fibrillation Effect on QualiTy-of-Life Questionnaire (AFEQT)	—

Countries

Japan

Contacts

Public ContactNobuhiro Ikemura

Keio University School of Medicine Department of Cardiology

ikemu0129@keio.jp03-5843-6702

Outcome results