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临床试验/NCT03842319
NCT03842319已完成不适用

Impact of MEditerranean Diet, Inflammation and Microbiome on Plaque Vulnerability and Microvascular Dysfunction After an Acute Coronary Syndrome. A Randomized, Controlled, Mechanistic Clinical Trial.

Consorcio Centro de Investigación Biomédica en Red (CIBER)2 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2019年5月14日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
100
试验地点
2
主要终点
Fibrous cap thickness change

研究概览

简要总结

In the MEDIMACS project, the investigators will use a randomized clinical-trial design to address the effects of mediterranean diet on atherosclerotic plaque vulnerability and coronary endothelial function in order to decipher complex interplays between diet, microbiome, immunological and metabolic responses and coronary atherosclerosis. The investigators will focus on patients after an episode of acute coronary syndrome and use state-of-the-art techniques to address atherosclerotic plaque composition and coronary endothelial function. A number of different -omic approaches will be used to address effector pathways. The insights provided by this study will allow identifying potential new dietary, microbiota and/or metabolic targets for the treatment of atherosclerosis

详细描述

Coronary atherosclerosis is a leading cause of mortality and disability worldwide. Continuous efforts are needed to improve secondary prevention and understand the mechanism underlying disease progression. Based on primary prevention trials, a potential benefit of the Mediterranean diet after an acute coronary syndrome can be anticipated. The integrated microbiome-mediated/ immunologic and metabolic pathways by which the Mediterranean diet modifies cardiovascular risk remain mostly unknown. Intestinal and oral dysbiosis is involved in the pathogenesis of atherosclerosis and microbiome dynamics may account for some of the observed benefits of Mediterranean diet. The first objective of the trial is to evaluate the effects of a well-controlled Mediterranean diet intervention on atherosclerotic plaque vulnerability and coronary endothelial dysfunction after an episode of acute coronary syndrome. The second objective is to decipher the interplays among diet, microbiota, immunity and metabolism responsible for the observed effects. The investigators propose a randomized mechanistic clinical trial, using state-of-the-art efficacy read-outs. The multidisciplinary consortium includes highly experienced cardiologists, nutritionists and experts in translational research in immunology, microbiomics, genomics, proteomics, metabolomics and metagenomics. This study will provide valuable insights to identify potential microbiome therapeutic targets for coronary artery disease.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Single (Investigator)

盲法说明

Non-intervention or MedDiet intensive intervention group assignment will be made through an automated system. Each patient will be assigned a patient identification number that should appear on all eCRF pages (electronic "case report"), source documents and laboratory data. All researchers involved in the measurement of data, analysis and allocation of results will be blind. The MedDiet intensive intervention will be blind to the evaluation of the endpoints (the research team in charge of the measurement, analysis and awarding of the results will be blind). The samples will be coded and anonymously analyzed by each research team

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

  • Adult patients undergoing cardiac catheterization for an acute coronary syndrome.
  • At least 1 non-causal lesion in a coronary segment with a stenosis diameter between 40-70% that will not be submitted to intervention during the revascularization procedure.
  • Disposition and possibility to modify the diet.
  • With the ability to track and answer questionnaires.
  • Signature of informed consent for the study

排除标准

  • TIMI score <3 in the injury
  • Reference lesion with diameter <2.0 mm
  • LV ejection fraction (EF) less than 45%.
  • Active systemic infection
  • Active periodontal disease
  • Chronic inflammatory disease
  • Active treatment with corticosteroids or immunomodulators
  • Renal insufficiency with glomerular filtration less than 30 mL / min
  • Severe hepatic insufficiency (liver cirrhosis in Child B or C stages).
  • Comorbidity with life expectancy of less than one year

结局指标

主要结局

Fibrous cap thickness change

时间窗: 12 months

Change in the thickness of the fibrous layer of the atheroma plaque in the non-culprit vessel measured by optical coherence tomography at 12 months.

次要结局

  • Intestinal microbiota composition changes(12 months)
  • Adaptive immune system status changes(12 months)
  • Faecal metabolome profiling changes(12 months)
  • Blood protein profiling changes(12 months)
  • Innate immune system status changes(12 months)
  • Faecal protein profiling changes(12 months)
  • Blood metabolome profiling changes(12 months)
  • Endothelial dysfunction(12 months)
  • Oral microbiota composition changes(12 months)
  • Urine metabolome profiling changes(12 months)

研究者

发起方
Consorcio Centro de Investigación Biomédica en Red (CIBER)
申办方类型
Other Gov
责任方
Sponsor

研究点 (2)

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