Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
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.
Prospective, open label, multicenter randomized clinical trial
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| dual anti-platelet therapy at least 6 months | Active Comparator |
| |
| dual anti-platelet therapy 3months or less | Experimental |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| dual anti-platelet therapy at least 6 months | Drug | Patients enrolled in dual antiplatelets at least 6 months arm would be administered with aspirin 100mg plus clopidogrel 75mg or prasugrel 10mg once daily for at least 6 months after randomization. Clopidogrel or prasugrel should be maintained after 6 months. |
| Measure | Description | Time Frame |
|---|---|---|
| Net Clinical adverse event (NACE) | A composite of all cause death, myocardial infarction, stent thrombosis, stroke, major bleeding (BARC 3,5) | 1 year |
| Measure | Description | Time Frame |
|---|---|---|
| The rate of Each component of NACE | all cause death, myocardial infarction, stent thrombosis, stroke, major bleeding (BARC 3,5) | 1 year |
| The rate of Cardiovascular death | 1 year |
Not provided
Inclusion Criteria:
Exclusion Criteria:
Not provided
Not provided
Not provided
Not provided
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Jung-Sun Kim, MD, PhD, FESC | Contact | 82)-2)-2228-8457 | KJS1218@yuhs.ac |
| Name | Affiliation | Role |
|---|---|---|
| Jung-Sun Kim, MD, PhD, FESC | Severance Hospital | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Division of Cardiology, Yonsei Cardiovascular Hospital, Yonsei University College of Medicine | Recruiting | Seoul | South Korea |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 41932491 | Derived | Jin IT, Lee SH, Yun KH, Kim W, Shin S, Jang JY, Cho DK, Cha JJ, Kang TS, Lee JH, Cho YK, Heo JH, Ahn SG, Lee J, Lee YJ, Lee SJ, Hong SJ, Ahn CM, Kim BK, Ko YG, Choi D, Hong MK, Jang Y, Kim JS. Optimal antiplatelet strategy in patients with advanced chronic kidney disease undergoing drug-eluting stent implantation: Design and rationale of the randomized ADAPT-CKD trial. Am Heart J. 2026 Aug;298:107437. doi: 10.1016/j.ahj.2026.107437. Epub 2026 Apr 1. |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
|
| dual anti-platelet therapy 3months or less | Drug | Patient enrolled in the dual antiplatelet therapy less than 3 months arm would be administered with aspirin 100mg plus clopidogrel 75mg or prasugrel 10mg once daily for less than 3 months after randomization. After 3 months clopidogrel or prasugrel should be maintained. |
|
| The rate of Major adverse cardiovascular events (MACE) | A composite of cardiovascular death, myocardial infarction, stent thrombosis or target vessel revascularization | 1 year |
| The rate of Composite ischemic outcomes | A composite of cardiovascular death, myocardial infarction, stent thrombosis or ischemic stroke | 1 year |
| The rate of major or clinically relevant nonmajor bleeding | BARC type 2,3,5 bleeding | 1 year |
| Fatal bleeding | 1 year |
| Intracranial hemorrhage | 1 year |
| The rate of Target lesion revascularization | 1 year |
| The rate of Target vessel revascularization | 1 year |
| The rate of Subgroup analysis of primary endpoint, key secondary efficacy, safety endpoint and, revascularization according to the CKD stage (lllb vs. IV or V) | 1 year |
| The rate of Subgroup analysis of primary endpoint, key secondary efficacy, safety endpoint and, revascularization according to the clinical presentation (chronic coronary syndrome vs. acute coronary syndrome) | 1 year |
| he rate of Subgroup analysis of primary endpoint, key secondary efficacy, safety endpoint and, revascularization according to the type of Stent (polymer-free vs. durable-polymer) | 1 year |
| ID | Term |
|---|---|
| D051436 | Renal Insufficiency, Chronic |
| ID | Term |
|---|---|
| D051437 | Renal Insufficiency |
| D007674 | Kidney Diseases |
| D014570 | Urologic Diseases |
| D052776 | Female Urogenital Diseases |
| D005261 | Female Urogenital Diseases and Pregnancy Complications |
| D000091642 | Urogenital Diseases |
| D052801 | Male Urogenital Diseases |
| D002908 | Chronic Disease |
| D020969 | Disease Attributes |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
Not provided
Not provided
| ID | Term |
|---|---|
| D000080903 | Dual Anti-Platelet Therapy |
| ID | Term |
|---|---|
| D004359 | Drug Therapy, Combination |
| D004358 | Drug Therapy |
| D013812 | Therapeutics |
Not provided
Not provided