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A randomized controlled pilot trial of Optimal Regimen of anti-platelet and oral anticoagulation therapy In atrial fibrillation patients undergoing pErcutaneous coronary iNTervention at Oriental resigon

A randomized controlled pilot trial of Optimal Regimen of anti-platelet and oral anticoagulation therapy In atrial fibrillation patients undergoing pErcutaneous coronary iNTervention at Oriental resigon

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0003298
Enrollment
60
Registered
2018-10-26
Start date
2018-11-19
Completion date
Unknown
Last updated
2021-01-28

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

Conditions

None listed

Interventions

Drug : In, atrial fibrillation patient has been percutaneous coronary intervention performed patient low-intensity therapy(aspirin 100mg + prasugrel 5mg + edoxaban 30mg) and standard therapy (aspirin

Sponsors

Chonnam National University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)Patients aged 18 to 75 years of age visiting with symptoms of non-valvular atrial fibrillation 2)Patients weighing more than 60 kg 3)CHA2DS2-VASc score = 1 embolism stroke high risk patient 4)Patients who voluntarily signed up for clinical trials 5)Patient who has not detected an atrial thrombus in the Transthoracic Echocardiography 6)Patients who receive stent insertion due to coronary artery disease

Exclusion criteria

Exclusion criteria: 1)Atrial fibrillation patient with reversible cause 2)valvular atrial fibrillation patients 3)Patients who are overreacting to aspirin's principal or component 4)Patients who are overreacting to the clopidogrel principal or component. 5)Patients who overreact to the principal or component of a prasugrel 6)Patients who are overreacting to the warfarin principal or component 7)Patients who overreact to the principal or the component in an edoxaban 8)creatinine clearnce< 30 ml/min Severe renal disease Patient 9)Ischemic and hemorrhagic strokes,transient ischemic attack history patient 10)Clinically significant bleeding patient 11)Patients with increased risk of bleeding due to the following diseases -The latest history of gastrointestinal ulcers. -Recent history of intracranial or intracerebral hemorrhage -Spinal cord or intracerebral vascular abnormalities -Recent brain or spinal cord injury -have esophageal varices -there is a vascular aneurysm -Malignant tumors with a high risk of bleeding 12)Women who are scheduled or confirmed pregnant or lactating

Design outcomes

Primary

MeasureTime frame
major bleeding;major adverse cardio cerebral events

Secondary

MeasureTime frame
minor bleeding;cardiac death;myocardial infarction;cerebral infarction;systemic thromboembolism

Countries

Korea, Republic of

Contacts

Public Contactyuri KIM

Chonnam National University Hospital

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026