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临床试验/NCT06886724
NCT06886724尚未招募不适用

A Study on the Role of Ligilactobacillus Salivarius LS97 in Modulating Gut Microbiota and Immune System Function

Wecare Probiotics Co., Ltd.1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2025年3月10日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
40
试验地点
1
主要终点
Change in the composition of fecal microbiota before and after intervention.

研究概览

简要总结

Evaluate the effectiveness and safety of Ligilactobacillus salivarius LS97 as a food supplement compared to a placebo in improving intestinal and immune functions in healthy adults.

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
Double (Participant, Investigator)

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Willing to undergo 3 follow-up visits during the intervention period
  • •Be willing to provide blood, urine and stool samples 2 times during the intervention period
  • •Good eyesight, can read and write, can wear glasses
  • •Have good hearing and be able to hear and understand all instructions during the intervention

排除标准

  • •Digestive diseases, mainly gastrointestinal diseases (celiac disease, ulcerative colitis, Crohn's disease)
  • •Have a serious neurological condition (epilepsy, stroke, severe head trauma, meningitis in the last 10 years, brain surgery, brain tumor prolonged coma - not including general anaesthesia)
  • •Have received/are receiving treatment for the following mental disorders: alcohol/drug/substance abuse dependence, schizophrenia psychosis, bipolar disorder
  • •Take medication for depression or low mood
  • •Internal organ failure (heart, liver or kidney failure, etc.)
  • •Have received radiation or chemotherapy in the past
  • •have undergone a general anesthesia procedure/procedure within the past three years, or plan to undergo a general anesthesia procedure/procedure within the next 3 months during this trial period
  • •Have had hepatitis (hepatitis B, hepatitis C), HIV or syphilis in the past

研究组 & 干预措施

Placebo group

Placebo Comparator

Every day to give 3 g maltodextrin intervention for 8 weeks.

干预措施: Placebo (Dietary Supplement)

Probiotic group

Active Comparator

Intervention with Ligilactobacillus salivarius LS97 (30 billion CFU/day, 3g) was administered daily for 8 weeks.

干预措施: Probiotic (Dietary Supplement)

结局指标

主要结局

Change in the composition of fecal microbiota before and after intervention.

时间窗: Week 0 and Week 8

Analyzed by 16S rRNA sequencing.

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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