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临床试验/NCT02194686
NCT02194686已完成4 期

Cilostazol Enhances the Number and Functions of Circulating Endothelial Progenitor Cells Mediated Through Multiple Mechanisms in Patients With High Risk for Cardiovascular Disease

National Cheng-Kung University Hospital1 个研究点 分布在 1 个国家目标入组 71 人开始时间: 2013年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
71
试验地点
1
主要终点
Circulating EPCs Number

研究概览

简要总结

  1. The number and function of circulating endothelial progenitor cells (EPCs) are inversely associated with coronary risk factors and atherosclerotic diseases.
  2. This double-blind, randomized, placebo-controlled trial to evaluate the effects of cilostazol on human early EPCs and endothelial function as well as the potential mechanisms of action in patients with high risk for cardiovascular disease.

详细描述

  1. titration of drugs

  2. run-in period: eligible subjects are screened and baseline blood samples are obtained

  3. study period: 12 weeks

  • subjects with cilostazol and subjects with dummy placebo
  • On the first day after the end of the study period, the follow-up data are obtained by the same procedure
  1. blood sampling and measurement of serum biomarkers
  • obtained from peripheral veins in all study subjects at the run-in period and the end of the treatment period of the study
  • sent for isolation, cell culture, and assays of human EPCs
  • also stored for enzyme-linked immunosorbent assay (stromal cell derived factor-alfa1, adiponectin, soluble thrombomodulin, vascular endothelial growth factor)
  1. assays of human EPCs

  2. colony formation by EPCs

  3. quantification of EPCs and apoptotic endothelial cells

  4. chemotactic motility, proliferation/viability and apoptosis assays

  5. measurement of flow-mediated dilatation (FMD) of left brachial artery by sonography

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

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

入选标准

  • high-risk patients who have at least one of the following situations without pre-existing cardiovascular disease including peripheral artery disease or coronary artery disease:
  • type 2 diabetes mellitus
  • metabolic syndrome
  • stage 3 (or more advanced) chronic kidney disease
  • 2 or more coronary risk factors (male > 45 years or female > 55 years, hypertension, tobacco smoking, hyperlipidemia, family history of cardiovascular disease)

排除标准

  • ankle-brachial index less than 0.9 or more than 1.3 in one or both legs
  • significant stenosis (more than 50% as compared to reference vessel) in peripheral artery on image study
  • symptoms suggesting peripheral artery disease in at least one leg
  • clinical or electrocardiographic evidence of coronary artery disease
  • clinical evidence of cerebrovascular disease
  • severe liver dysfunction (transaminases >10 times of upper normal limit, history of liver cirrhosis, or hepatoma)
  • left ventricular ejection fraction (<50% by echocardiography)
  • documented active malignancy
  • chronic inflammatory disease
  • known drug allergy history for cilostazol
  • current use of cilostazol or any other cAMP-elevator
  • premenopausal women

研究组 & 干预措施

Cilostazol

Active Comparator

One tablet (100 mg) twice per day for 12 weeks

干预措施: Cilostazol (Drug)

Dummy Placebo

Placebo Comparator

One tablet twice per day for 12 weeks

干预措施: Dummy Placebo (Drug)

结局指标

主要结局

Circulating EPCs Number

时间窗: 3 months

Peripheral blood mononuclear cells (one million cells in each) are suspended in 100 µL phosphate-buffered saline and incubated for 30 min with monoclonal antibodies against human peridinin chlorophyll protein-conjugated cluster of differentiation antigen-45, phycoerythrin-conjugated anti-human cluster of differentiation antigen-34 antibody and anti-human kinase insert domain receptor (KDR) antibody conjugated with Alexa Flour 647. Cells are washed and analyzed on a FACSCalibur flow cytometer with 100,000 events in the lymphocyte gate. EPCs, which are defined as negative for cluster of differentiation antigen-45 and positive for cluster of differentiation antigen-34 and KDR. Based on the peripheral blood mononuclear cell counts, the absolute number of circulating EPCs/µL is calculated.

次要结局

  • Viability (Proliferation) of EPCs(3 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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