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Antiplatelet therapy for prevention of atherosclerosis in chronic kidney disease: A perspective, multi-center randomized controlled trial

Antiplatelet prophylaxis for atherosclerosis in chronic kidney disease: a multicenter, randomized, pacebo-controlled trial

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900021393
Enrollment
Unknown
Registered
2019-02-18
Start date
2019-04-01
Completion date
Unknown
Last updated
2019-02-25

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

Conditions

chronic kidney diseases

Interventions

Sponsors

The Second Affiliated Hospital of the Amy Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
14 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. renal impairment 3 months, with or without decreased glomerular filtration rate (GFR). Renal damage refers to the abnormal structure or function of the kidney, manifested as one of the following: 1) pathological examination abnormalities; 2) eGFR<60ml/min/1.73m2 3 months, with or without renal damage.EGFR =169 Scr-0.608 CysC-0.63 Age-0.157 (0.83 if female); 2. For patients with CKD stage 3-5 (non-dialysis), age 14-65 years old (including 14 and 65 years old), gender, ethnicity is not limited; 3. The ultrasound of the cervical blood vessels showed no cervical vascular plaque and no atherosclerosis. 4. patients signed informed consent.

Exclusion criteria

Exclusion criteria: 1. unable or unwilling to complete the required process for the research; 2. participating in other interventional clinical trials; 3. women who are pregnant or lactating; 4. previous diagnosis of CKD with cardiovascular disease or previous cardiovascular disease patients, it shall clearly diagnosis myocardial infarction, heart failure, cerebral hemorrhage and other serious cardiovascular and cerebrovascular complications; 5. NYHA level III or IV heart failure, that is, there is a basic heart disease, physical activity was significantly limited, less than the general physical activity or rest state may appear fatigue, palpitations, asthma or angina symptoms; 6. Lilitide cirrhosis; 7. Therefore HIV infection or AIDS; 8. In the past 2 years due to malignant tumor chemotherapy or alkylation agent treatment; 9. kidney transplant patients; 10. on the existence of deep venous thromboembolism before inclusion; 11. In the prior to entering the group, in the long-term use of aspirin or hydroclopidogrel, or in the recent three months in the short use of aspirin or hydroclopidogrel; 12. the patients with active bleeding or coagulation dysfunction.

Design outcomes

Primary

MeasureTime frame
Atherosclerosis;

Secondary

MeasureTime frame
Complex cardiovascular events;all-cause mortality;A 50% drop in eGFR;

Countries

China

Contacts

Public ContactZhao Jinghong

The Second Affiliated Hospital of the Amy Medical University

zhaojh@tmmu.edu.cn+86 13668007369

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 16, 2026