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临床试验/NCT03543774
NCT03543774Unknown4 期

Lipid-lowering Regimes Improve Oxidative Stress, Tryptophan Degradation in Hypercholesterolemia Chronic Kidney Disease Patients

Hue University of Medicine and Pharmacy1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2018年6月15日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
入组人数
30
试验地点
1
主要终点
To measure the serum level of Taurine, Tryp, and Kyn in Vietnamese CKD population and in healthy persons at the base time.

研究概览

简要总结

This study aims to determine the mechanisms underlying dyslipidemia in chronic kidney disease (CKD) and effect of lipid-lowering therapies in patients with CKD via parameters of lipid, oxidative stress, tryptophan delegation as well as renal function and side effects. Thirty 3,4 CKD patients with low-density lipoprotein (LDL) > 100 mg/mL (2,59mmol/l), randomly receive three different LDL lipid-lowering therapies: Simvastatin (40 mg/day) or ezetimibe/simvastatin combination (10/20 mg/day or 10/40 mg/day).

详细描述

The prevalence of chronic kidney disease (CKD) in Vietnamese population is increasing along with hypertension and diabetes. In CKD patient, cardiovascular disease (CVD) is the leading cause of mortality. The lipidemic disorder is one of the CV risk factors in CKD but it was not fully concerned in Viet Nam.

Hypocholesterolemia therapy has shown many benefits; however, its effects on OS and endothelial function are still not fully evidenced.

In clinical practice, physicians always concern the effects and safety before giving the prescription. However, despite the high frequency of statin treatment, only 1/3 of CKD patients achieved the LDL-C goal. Whether high-dose of statins mono-therapy is more effective in LDL-C lowering is still unclear, but are associated with a high rate of hepatotoxicity, myopathy.

Lowering LDL-C with statin mono-therapy and statin/ezetimibe combination reduces the risk of CVD in population without kidney disease. Which Cholesterol-lowering therapies are suitable for stage 3,4 CKD patients in term of e-GFR reduction and side effects? There is no data related to this field in the Vietnamese CKD population.

Thus, more advanced lipid-lowering therapies and a better understanding of the mechanism is needed for treatment strategy of hyperlipidemia in Vietnamese patients with CKD.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Ages Eligible for Study:
  • ≥ 50 years old but not treated with chronic dialysis or kidney transplantation
  • In adults aged 18-49 years with CKD but not treated with chronic dialysis or kidney transplantation, statin treatment in people with one or more of the following: known coronary disease (myocardial infarction or coronary revascularization); diabetes mellitus; prior ischemic stroke; estimated 10-year incidence of coronary death or non-fatal myocardial infarction > 10%.
  • CKD in the 3,4 stage: (e-GFR: 15-60 ml/min/1.73 m2)
  • CKD proteinuria (defined as Creatinine clearance >20 ml/min/1.73 m2 combines with urinary protein excretion rate >300mg/24 h)
  • LDL cholesterol concentration > 100 mg/dl (2,59 mmol/l)

排除标准

  • In adults with dialysis-dependent CKD
  • Heart failure (New York Heart Association class III or more)
  • Previous or concomitant treatment with corticoids, statin, immunosuppressive agents, vitamin B6, B12, folate.
  • Pregnancy
  • Patients who do not agree to participate the research
  • Patients are unable to understand the purposes and the risks of the study

研究组 & 干预措施

simvastatin treatment

Active Comparator

干预措施: Simvastatin 40mg (Drug)

EZE/simvastatin 10/20 mg treatment

Sham Comparator

干预措施: Ezetimibe/simvastatin 10/20 mg/day (Drug)

EZE/simvastatin 10/40 mg treatment

Sham Comparator

干预措施: Ezetimibe/simvastatin 10/40 mg/day (Drug)

结局指标

主要结局

To measure the serum level of Taurine, Tryp, and Kyn in Vietnamese CKD population and in healthy persons at the base time.

时间窗: At the base time

The serum level of Taurine, Tryp, and Kyn will be measured in micromol/L

To measure the serum level of TC, LDL-C, HDL-C, TG, Creatinine, uric acid, and allantoin in Vietnamese CKD population and in healthy persons at the base time.

时间窗: At the base time

The serum level of TC, LDL-C, HDL-C, TG, Creatinine, uric acid, and allantoin will be measured in mg/dL.

To measure the number of red blood cell, white blood cell and platelet in Vietnamese CKD population and in healthy persons at the base time.

时间窗: At the base time

The number of red blood cell, white blood cell, and platelet will be measured in number/L

To measure the serum level of SGOT, SGPT, and Creatinin Kinase in Vietnamese CKD population and in healthy persons at the base time.

时间窗: At the base time

The serum level of SGOT, SGPT and Creatinin Kinase will be measured in Units/L

To measure the level of Albuminuria and urine Creatinine in Vietnamese CKD population and in healthy persons at the base time.

时间窗: At the base time

The serum level of Albuminuria and urine Creatinine will be measured in mg/dL

To measure the serum level of MDA in Vietnamese CKD population and in healthy persons at the base time.

时间窗: At the base time

The serum level of MDA will be measured in nmol/L

次要结局

  • To measure the serum level of TC, LDL-C, HDL-C, TG, Creatinine, uric acid, and allantoin in Vietnamese CKD population at 4th, 8th, 12th month.(at 4th, 8th and 12th month)
  • To measure the number of red blood cell, white blood cell and platelet in Vietnamese CKD population at 4th, 8th, 12th month.(at 4th, 8th and 12th month)
  • To measure the level of Albuminuria and urine Creatinine in Vietnamese CKD population at 4th, 8th, 12th month.(at 4th, 8th and 12th month)
  • To measure the serum level of Taurine, Tryp, and Kyn in Vietnamese CKD population at 4th, 8th, 12th month.(at 4th, 8th and 12th month)
  • To measure the serum level of MDA in Vietnamese CKD population at 4th, 8th, 12th month.(at 4th, 8th and 12th month)
  • To measure the serum levels of SGOT, SGPT and Creatinine Kinase in Vietnamese CKD population at 4th month, 8th month and the 12th month(at 4th, 8th and 12th month)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Duong Thi Ngoc Lan

Principal Investigator, Physician, Master degree

Hue University of Medicine and Pharmacy

研究点 (1)

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