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临床试验/NCT04390347
NCT04390347已完成不适用

Daily Intake of Lactobacillus Casei Shirota (LcS) Modulates Intestinal Permeability and Decreases Circulating Levels of Endotoxin That Associate With Both Cardiovascular and All-cause Mortality in Haemodialysis Patients

University of Leicester1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2020年9月21日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
60
试验地点
1
主要终点
Blood circulating endotoxin concentration

研究概览

简要总结

This is a double-blind randomised controlled trial where participants will be randomised to either twice daily 65ml of Lactobacillus casei Shirota for six months or a matched placebo.

详细描述

Intervention

The intervention product (Yakult) (supplied as fermented milk) and placebo will be delivered in sealed pots of 65 mL with date stamped expiry. Yakult contains Lactobacillus casei Shirota (a minimum of 6.5 × 10 9 live cells of Lactobacillus casei Shirota are contained in each pot). The pots will be stored at 4-7 °C (domestic refrigerator) on premises at University Hospital of Leicester and the University of Leicester until provided to participants. These products have a shelf life of four weeks but fresh deliveries will be sent every two weeks. They will be stored at approximately seven degrees Celsius (refrigerated at the University and subsequently, after delivery to participants, in domestic refrigerators) in a restricted area where only members of the research team will have access to them. Participants will have supplies provided to them in person every two-weeks and will be required to ingest two pots of Yakult, every day for six months. Participants will be instructed to ingest one 65ml pot in the morning (prior to breakfast) and one bottle in the evening (prior to an evening meal). They will also be instructed to avoid any other dietary supplement aimed at modulating the gut microbiota during the six month intervention period. Researchers will keep a log of the amount of pots supplied to participants and will visit the participants at the haemodialysis unit to supply more pots.

Placebo

The placebo will be indistinguishable (identical in taste and colour but will not contain Lactobacillus casei Shirota) to both participants and trial investigators. It will be stored and provided in exactly the same manner as the intervention product.

Compliance

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)

盲法说明

Placebo.

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

  • Be a prevalent haemodialysis patient (>3 months)
  • Age 18 years or older
  • Able and willing to give informed consent
  • Sufficient understanding of English to understand the patient information sheet and complete questionnaires

排除标准

  • Aged <18 years
  • Unable or unwilling to give informed consent
  • Unlikely to remain on haemodialysis for the 6-month duration of the trial (e.g. planned transplantation)
  • Already taking a regular pre- or pro-biotic supplement or other dietary supplement aimed at modulating the gut microbiota
  • Any of the following conditions:
  • Documented allergy or intolerance to milk protein (e.g. lactose intolerance, milk/dairy allergy)
  • Autoimmune disease (e.g. systemic lupus erythematosus)
  • Inflammatory bowel disease (e.g. Crohn's colitis)
  • Diagnosed infectious illness within the previous 30-days
  • Prescribed any of the following medication:
  • Antibiotics or anti-viral medications within the previous 30-days
  • Steroids or other immunosuppressive agents -

结局指标

主要结局

Blood circulating endotoxin concentration

时间窗: 6 months

Gut derived toxic particle

次要结局

  • Faecal elastase concentration(6 months)
  • Salivary immunoglobulin A concentration(6 months)
  • Faecal p-cresol concentration(6 months)
  • Salivary lysozyme concentration(6 months)
  • Blood circulating interleukin-6 concentration(6 months)
  • Blood circulating high sensitivity c-reactive protein concentration(6 months)
  • Blood circulating monocyte chemoattractant protein (MCP)-1 concentration(6 months)
  • Faecal bacterial load(6 months)
  • Faecal bacterial diversity(6 months)
  • Faecal indole concentration(6 months)
  • Faecal phenol concentration(6 months)
  • Faecal calprotectin concentration(6 months)
  • Blood circulating interleukin-10 concentration(6 months)
  • Blood circulating indoxyl sulphate concentration(6 months)
  • Faecal ammonia concentration(6 months)
  • Blood circulating p-cresyl sulphate concentration(6 months)
  • Blood circulating E-selectin concentration(6 months)
  • Blood circulating P-selectin concentration(6 months)
  • Blood circulating tumour necrosis factor alpha concentration(6 months)
  • Blood circulating intercellular cell-adhesion molecule 1 concentration(6 months)
  • Blood circulating vascular cell adhesion molecule 1 concentration(6 months)
  • Blood circulating Irisin(6 months)
  • EQ-5D-5L(6 months)
  • Gastrointestinal Symptom Rating Scale(6 months)
  • Blood circulating interleukin-17 concentration(6 months)
  • Blood circulating interleukin-8 concentration(6 months)
  • Blood circulating RANTES concentration(6 months)
  • Blood circulating MicroRNA's(6 months)
  • Blood circulating C-terminal agrin fragment (CAF)(6 months)
  • Blood circulating Brain derived neurotrophic factor (BDNF)(6 months)
  • Kidney disease quality of life instrument (KDQOL)(6 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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