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临床试验/NCT03430726
NCT03430726Unknown不适用

The ProbGut Study: Effects of Probiotics on the Gut Microbiota of Healthy Children

McMaster University2 个研究点 分布在 1 个国家目标入组 42 人开始时间: 2018年3月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
42
试验地点
2
主要终点
Levels of Fecal Biomarkers - beta-defensins-2 (hBD-2)

研究概览

简要总结

In adults, probiotics have been shown to have no effect on the microbial composition and the beneficial effects are only transient. However, the gut microbiota of young children is less stable and more impressionable. The aim of this study is to examine the effects of probiotics on the developing microbiota in early life and to determine whether a young child's microbiota may be less resilient to probiotic-induced changes and possibly resulting in longer lasting probiotic effects compared to adults.

详细描述

Probiotics are live microorganisms that have been associated with health benefits. However, probiotic effects have not been shown to persist beyond discontinuation of use in adults. The intake of probiotics during the critical window of gut microbiota development in young children, however, may allow for a longer duration of persistence of probiotic bacteria and more stable changes in microbial composition possibly resulting in stable engraftment of the probiotic strains. This study aims is to examine the effect of a 14-day course of a commercially available probiotic yogurt drink on the composition, diversity, and changes in immune biomarkers (e.g. human beta-defensin-2 and calprotectin) of the gut microbiota of healthy children. As well, to assess whether the probiotic strains persists after discontinuation of intake and whether engraftment occurs. By understanding the impact of probiotics on the gut microbiota, we will better understand the mechanism by which probiotics exert their beneficial effects. This may help guide probiotic selection based on the potential short- and long-term effects on the commensal microbiota.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Other
盲法
None

入排标准

年龄范围
1 Year 至 3 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Participants will be healthy children between 1 to 3 years of age.
  • Participants will be considered healthy on entry into the study if they did not have a history of chronic gastrointestinal issues, including chronic or frequent episodes of diarrhea (>3 bowel movements/day for 3 consecutive days) during the month prior to enrolment.
  • Mother of participant is able to communicate in English (read, write, speak), as she will be required to provide her personal and medical history.

排除标准

  • Lactose or milk protein intolerance, or strawberry anaphylaxis, or allergies to dried citrus pulp, or any other components of the study product.
  • Immuno-compromised children (e.g. heart or kidney transplant, complex care, sickle cell disease) or those on immunosuppressive agents (e.g. chemotherapy agents, oral prednisone).
  • Children with known or potentially compromised gut integrity (e.g. short gut, Inflammatory Bowel Disease, Celiac, nasogastric, naso-jejunal or gastrostomy tube).
  • Children admitted to a medical or surgical subspecialty unit.
  • Children on antimicrobial therapy within 30 days prior to enrolment.
  • Children on an alternative probiotic within 30 days prior to enrolment.

研究组 & 干预措施

Healthy Kids Probiotic Yogurt Drink Group

Experimental

Healthy children will be given a commercially available yogurt drink containing a multi-strain probiotic, Bio-Kidz® (12.5 billion CFU/98g; Lactobacillus acidophilus CL1285®, Lactobacillus casei LBC80R® and Lactobacillus rhamnosus CLR2®), daily for 14 days.

干预措施: Probiotic yogurt drink (Other)

结局指标

主要结局

Levels of Fecal Biomarkers - beta-defensins-2 (hBD-2)

时间窗: Baseline, 21 days, 30 days, and 90 days

Change in levels of beta-defensins-2 (hBD-2)

Levels of Fecal Biomarkers - Fecal Calprotectin

时间窗: Baseline, 21 days, 30 days, and 90 days

Change in levels of Fecal Calprotectin

Composition and Diversity of Gut Microbiota

时间窗: Baseline, 30 days and 90 days

Change in microbial community (e.g. alpha and/or beta diversity) post-probiotic

次要结局

  • Duration of Persistence (DOP)(90 days post intervention)
  • Occurrence of Adverse Events(Through study completion, an average of 121 days.)

研究者

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

Kim Chau

Principal Investigator

McMaster University

研究点 (2)

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