Comparing Clopidogrel and Cilostazol for preventing cardiovascular issues in diabetics
Official title: Comparing Clopidogrel and Cilostazol in Type 2 Diabetes Patients With Carotid Atherosclerosis
Run by Seoul National University Bundang Hospital · NCT06402747 · Data updated 2026-11-12
This study is testing whether the medications Clopidogrel and Cilostazol can help prevent heart problems in adults with type 2 diabetes who have early signs of artery hardening.
Quick facts
| Phase | Phase 4 |
|---|---|
| Study type | Interventional |
| Ages | 19 Years and up |
| Sex | All |
| Enrollment | 120 (estimated) |
| Sponsor | Seoul National University Bundang Hospital Academic / other |
| Locations | 1 site (Seongnam-si, Gyeonggi-do) |
| Status | Recruiting |
| Started | April 16, 2024 |
| Main results expected | December 31, 2026 |
| Study ends | January 31, 2027 |
| Registry record updated | May 5, 2026 |
| Trial ID | NCT06402747 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are adults aged 19 and older with type 2 diabetes and a carotid intima-media thickness of 1.0mm or more.
✕Probably not a fit
Patients currently using antithrombotic or anticoagulant medications other than aspirin may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This clinical trial investigates the effectiveness of Clopidogrel and Cilostazol in preventing cardiovascular diseases among adults with type 2 diabetes who show early signs of atherosclerosis. Participants will undergo carotid ultrasound to measure carotid intima-media thickness, which helps assess their cardiovascular risk. The study aims to determine if these medications can inhibit the progression of carotid atherosclerosis in this high-risk population. By evaluating these treatments, the trial seeks to provide insights into their potential role in primary prevention strategies for cardiovascular complications in diabetics.
Why it matters
Potential benefit: If successful, this study could lead to improved prevention strategies for cardiovascular diseases in patients with type 2 diabetes.
How similar studies have gone: While the use of Clopidogrel and Cilostazol has been established for symptom control, their role in primary prevention for this specific population is still being explored, making this approach relatively novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Adults with diabetes aged 19 and older * Individuals with a carotid ultrasound cIMT (carotid intima-media thickness) of 1.0mm or more * Those who have not changed their combination therapy medications (including oral hypoglycemics, antihypertensives, and lipid-lowering drugs) in the last three months * Individuals with an HbA1c level of 10% or less * Those who have voluntarily signed the written consent form and agreed to participate in the study Exclusion Criteria: * Individuals currently using antithrombotic or anticoagulant medications other than aspirin * Individuals with bleeding or conditions that may increase the risk of bleeding, such as: * Hemophilia, capillary fragility, intracranial hemorrhage, upper gastrointestinal bleeding, urinary bleeding, hemoptysis, vitreous hemorrhage, etc * Active peptic ulcer, hemorrhagic stroke within the last 6 months, surgical operations within the last 3 months, proliferative diabetic retinopathy, uncontrolled hypertension * Patients who have had cerebrovascular or cardiovascular complications within the past 6 months (including stroke, transient ischemic attacks, myocardial infarction, unstable angina, coronary artery bypass graft, or percutaneous coronary intervention) * Patients with severe renal or hepatic diseases * Patients with congestive heart failure * Individuals with a history of hypersensitivity to the drug or its components * Pregnant women or women who may be pregnant * Women who are breastfeeding or plan to breastfeed during the study
Where it's running
-
Seoul National University Bundang Hospital
Seongnam-si, Gyeonggi-do, South Korea Recruiting
Study contacts
- Principal investigator: Soo Lim, MD. Ph.D. — Seoul National University Bundang Hospital
- Study coordinator: Soo Lim, MD. Ph.D.
- Email: limsoo@snu.ac.kr
- Phone: +82317877035
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Investigating body fat distribution and its impact on metabolic diseases in Japanese adults
This study looks at how the way body fat is distributed affects the risk of metabolic and heart diseases in Japanese adults.
-
Acute Blood Flow Restriction Walking in Type 2 Diabetes
This study tests whether adding blood flow restriction to treadmill walking affects immune cells in adults with type 2 diabetes.
-
Continuous Glucose Monitoring in Type 2 Diabetes Not on Insulin
This study tests whether using a continuous glucose monitoring system helps people with type 2 diabetes who aren’t using insulin to improve blood sugar control and quality of life.
-
Differentiating heart disease in autoimmune vs. type 2 diabetes
This study tests whether adult-onset autoimmune diabetes (AID/LADA) and type 2 diabetes (T2D) differ in how diabetic heart disease develops, using advanced heart imaging in people with AID, T2D, and healthy controls.
-
Lifestyle Metabotype Study B: Understanding Personalized Glucose Responses
This study tests how lifestyle, metabolism, and brain energy use relate to each person’s blood sugar response after meals, across people with and without prediabetes or type 2 diabetes.
-
Lifestyle Metabotype Study: How Daily Habits Shape Blood Sugar
This observational study tests whether personal lifestyle and biological factors can predict how a person’s blood sugar responds after meals.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.