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Recruiting NCT04708587

NCT04708587 Appropriate Duration of Anti-Platelet straTegy in Patients With Advance Chronic Kidney Disease After New Generation Drug Eluting Stents (ADAPT-CKD)

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Clinical Trial Summary
NCT ID NCT04708587
Status Recruiting
Phase
Sponsor Yonsei University
Condition Chronic Kidney Diseases
Study Type INTERVENTIONAL
Enrollment 900 participants
Start Date 2021-03-23
Primary Completion 2027-03-13

Trial Parameters

Condition Chronic Kidney Diseases
Sponsor Yonsei University
Study Type INTERVENTIONAL
Phase N/A
Enrollment 900
Sex ALL
Min Age 19 Years
Max Age 84 Years
Start Date 2021-03-23
Completion 2027-03-13
Interventions
dual anti-platelet therapy at least 6 monthsdual anti-platelet therapy 3months or less

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Brief Summary

The purpose of this prospective randomized clinical trial is to compare the clinical outcomes according to the duration of aspirin and clopidogrel or prasugrel with dual anti-platelet therapy after percutaneous coronary intervention in patients with advanced chronic kidney disease using a new generation drug eluting stents.

Eligibility Criteria

Inclusion Criteria: 1. Over 19 years old 2. Chronic Renal Failure Stage IIIb, IV, V (CKD-EPI eGFR \<45 / \<30 / \<15 or dialysis) 3. Patients treated with a new generation drug eluting stent. 4. Patients who signed consent form Exclusion Criteria: 1. Over 85 years old 2. Patients with high risk of bleeding 1) History of hemorrhagic stroke 2) Stroke, dementia or central nervous system damage within 1 year 3) Head trauma or brain surgery within 6 months 4) Tumor in the skull 5) If aortic dissection is suspected 6) Internal bleeding within 6 weeks 7) In case of active bleeding or bleeding disorder 8) In case of major surgery, trauma or bleeding within 3 weeks 3. Patients who need oral anticoagulant 4. Pregnant women or women of childbearing age 5. Life expectancy is less than 1 year 6. Patients with a history of intracranial bleeding 7. Moderate to severe hepatic impairment (Child-Pugh class B or C)

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