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Thromboembolic And Bleeding Risks During anticoaGulant trEatment in Asian paTients With Atrial Fibrillation (TARGET-AF)

Thromboembolic and Bleeding Risk During Anticoagulant Treatment in Asian Patents With Atrial Fibrillation

Status
Enrolling by invitation
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06874894
Acronym
NOAC
Enrollment
1021
Registered
2025-03-13
Start date
2022-05-25
Completion date
2026-08-30
Last updated
2025-12-29

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

Conditions

Fibrillation, Atrial

Keywords

Atrial Fibrillation, Stroke, Bleeding

Brief summary

This study was design to investigate the efficacy and safety of NOAC therapy in Koreans

Detailed description

East Asians have demonstrated a higher bleeding tendency compared to Western populations during an anticoagulation. Consequently, East Asians have been prescribed as a relatively weaker treatment regimens based on this evidence. Therefore, the TARGET-AF study aims to verify the efficacy and safety of NOAC therapy using biomarkers including TEG®-6S point-of-care device in Koreans

Interventions

None listed

Sponsors

Chung-Ang University Gwangmyeong Hospital
CollaboratorOTHER
Samsung Medical Center
CollaboratorOTHER
Korea University Ansan Hospital
CollaboratorOTHER
Kosin University Gospel Hospital
CollaboratorOTHER
Keimyung University Dongsan Medical Center
CollaboratorOTHER
Yuhan Corporation
CollaboratorINDUSTRY
Chung-Ang University Hosptial, Chung-Ang University College of Medicine
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Months to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients with documented AF on 12-lead ECG, Holter monitoring, or single-lead ECG recordings are eligible for enrollment. * Based on AF treatment Korean guideline 19, AF patients who require NOAC treatment or are currently on NOAC treatment (within the past 3 months) * Adults aged 18 or above who have provided consent for clinical information

Exclusion criteria

* Patients with moderate or severe mitral stenosis or mechanical prosthetic valve

Design outcomes

Primary

MeasureTime frameDescription
Clinical ischemic and hemorrhagic events12 monthsThe Rate of Ischemic stroke, systemic embolism, or myocardial infarction and ISTH (International Society on Thrombosis and Hemostasis) major/minor bleeding events

Secondary

MeasureTime frameDescription
Clinical other events12 monthsThe rate of Major Adverse Cardiovascular Events: Myocardial infarction, ischemic stroke, systemic embolism, and cardiovascular death (including bleeding).

Other

MeasureTime frameDescription
COVID-19 infection12 monthsThe rate of confirmation of COVID-19 infection and primary outcome

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026