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临床试验/NCT01218165
NCT01218165已完成早期 1 期

The Inflammaging Network: Bridging Low Grade Inflammation With Gut Microbiota and Intestinal Barrier Function in Elderly Humans

Charite University, Berlin, Germany2 个研究点 分布在 1 个国家目标入组 48 人开始时间: 2010年5月最近更新:
适应症

试验速览

阶段
早期 1 期
状态
已完成
入组人数
48
试验地点
2
主要终点
Pre/post-intervention change in hsCRP

研究概览

简要总结

Cardiovascular diseases (CVD) are the main cause of death in the European Union. A large part of the aging process, including immunosenescence, is explained by an imbalance between inflammatory and anti-inflammatory networks, wich results in the low grade chronic pro-inflammatory status termed inflammaging. It can contribute to a number of age-related chronic diseases (e.g. atherosclerosis, type 2 diabetes, Alzheimer disease, osteoporosis). Prevention or delay in onset of chronic diseases can potentially benefit a large segment of the elderly population. Now it is hypothesised that a probiotic drink can reduce low-grade inflammation through improvement of the gut barrier function and gut microbiota composition in elderly people with low-grade inflammation.

详细描述

Cardiovascular diseases (CVD) are the main cause of death in the European Union. A large part of the aging process, including immunosenescence, is explained by an imbalance between inflammatory and anti-inflammatory networks, wich results in the low grade chronic pro-inflammatory status termed inflammaging. It can contribute to a number of age-related chronic diseases (e.g. atherosclerosis, type 2 diabetes, Alzheimer disease, osteoporosis). Prevention or delay in onset of chronic diseases can potentially benefit a large segment of the elderly population. Now it is hypothesised that a probiotic drink can reduce low-grade inflammation through improvement of the gut barrier function and gut microbiota composition in elderly people with low-grade inflammation.

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
None

入排标准

年龄范围
65 Years 至 85 Years(Older Adult)
性别
Male
接受健康志愿者

入选标准

  • Men >65 years of age.
  • Body mass index: 22-34,9 kg/m²
  • non-smokers
  • Intervention trial:
  • hsCRP > 1 mg/L (Screening blood test)
  • normal blood count (Screening blood test)
  • normal ALAT, ASAT and serum creatinine levels (Screening blood test)

排除标准

  • any major non-organic disease, including malign diseases (haematological, inflammatory, metabolic,)
  • any major organ disease, including neoplastic diseases.
  • intake of antibiotics within the last 6 weeks
  • chronic therapy with analgetics (incl. acetylsalicylic acid)
  • chronic therapy with proton pump inhibitors
  • regular intake of probiotic bacteria products within the last 3 weeks
  • chronic anti-inflammatory therapy with NSARs or previous therapy within the last 20 days
  • subjects with expected non-compliance to protocol guidelines
  • subjects that participate in other trials

结局指标

主要结局

Pre/post-intervention change in hsCRP

时间窗: 6 weeks

Change (reduction) of hsCRP over a 6-week period in older persons.

次要结局

  • Intestinal permeability(6 weeks)
  • Stool: Stool: Real-Time-PCR(6 weeks)
  • Blood screening(6 weeks)
  • Muscle function(6 weeks)
  • Physical performance status(6 weeks)

研究者

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

Luzia Valentini

Research Scientist

Charite University, Berlin, Germany

研究点 (2)

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