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临床试验/NCT05840588
NCT05840588已完成不适用

Effect of Bifidobacterium Breve PRL2020 (an Amoxicillin-Clavulanate-Resistant Strain) on Gastrointestinal Symptoms and Gut Microbiota Composition in Children Treated With Amoxicillin or Amoxicillin/Clavulanate: Results of a Pediatric, Multicenter, Randomized, Controlled, Prospective Study

Liaquat University of Medical & Health Sciences1 个研究点 分布在 1 个国家目标入组 121 人开始时间: 2023年11月6日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
121
试验地点
1
主要终点
Incidence of antibiotic-associated diarrhea (AAD)

研究概览

简要总结

Amoxicillin or Amoxicillin/Clavulanic acid antibiotic therapy has been shown to be associated with disrupting the microbiota population particularly Bifidobacterium, which may have further GI clinical implications.

The present randomized clinical trial is aimed to assess if probiotic Bifidobacterium breve PRL2020 (Brevicillin®) can help modulate the Bifidobacterium population and its clinical implications after antibiotic Amoxicillin or Amoxicillin/Clavulanic acid antibiotic therapy.

详细描述

Treatment with Amoxicillin or Amoxicillin/Clavulanic acid is one of the most common antibiotic therapies used against various infections both in children and adults. These antibiotics can create an imbalance in the intestinal microbiota, altering its structure with a reduction in bacterial richness and, more specifically, in the abundance of bifidobacteria. This opened the window for further evaluations of the effect of this antibiotic combination on the composition of gut microbiota. The alteration can lead to intestinal symptoms such as pain, bloating, abdominal distension, flatulence, diarrhea, and constipation. In study by L. Mancabelli et al. (2021), Bifidobacterium breve PRL2020 has shown greatest resistance to Amoxicillin and Amoxicillin/Clavulanic acid. Currently available scientific data, however, have not yet analyzed the ability of B. breve PRL2020 to counteract the reduction of bifidobacteria that may occur in the human gut during the antibiotic therapy with Amoxicillin or Amoxicillin/Clavulanic acid, and neither its ability to avoid the consequent clinical relapse.

The purpose of this randomized, controlled (untreated group), prospective, multicentre, single-center, non-profit study will be to evaluate the efficacy and safety of the administration of Bifidobacterium breve PRL2020 (Brevicillin®) in pediatric patients (> 3 -12 years of age), treated with the antibiotic Amoxicillin or Amoxicillin/Clavulanic acid, in the improvement of the symptoms due to the pharmacological treatment and in the contrast of the fall of the Bifidobacterium cluster.

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
None

入排标准

年龄范围
3 Years 至 12 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Children aged between 3-12 years, of either gender, with a bacterial infection and the use of antibiotic therapy with Amoxicillin or Amoxicillin/clavulanic acid under a Physician's prescription.

排除标准

  • Presence of neurological, oncological (also past), malformative, and/or autoimmune pathology
  • Suspected or presumed allergy to the substance contained in the probiotic formula
  • Using any type of probiotic product in the three months before the enrollment or during the trial
  • Lack of parental consent to participate in the study

研究组 & 干预措施

Control

Active Comparator

Patients in this arm will receive only antibiotic Amoxicillin or Amoxicillin/Clavulanic acid.

干预措施: Antibiotic Treatment (Drug)

Probiotic Bifidobacterium breve PRL2020 (Brevicillin®)

Experimental

Patients in this arm will receive Probiotic Bifidobacterium breve PRL2020 (Brevicillin®) (20 billion CFU) 2 sticks/day for 7-10 days (according to antibiotic prescription)in addition to the antibiotic Amoxicillin or Amoxicillin/Clavulanic acid (antibiotic doses: 2-3/day according to physician prescription).

干预措施: Antibiotic Treatment (Drug)

Probiotic Bifidobacterium breve PRL2020 (Brevicillin®)

Experimental

Patients in this arm will receive Probiotic Bifidobacterium breve PRL2020 (Brevicillin®) (20 billion CFU) 2 sticks/day for 7-10 days (according to antibiotic prescription)in addition to the antibiotic Amoxicillin or Amoxicillin/Clavulanic acid (antibiotic doses: 2-3/day according to physician prescription).

干预措施: Probiotic Bifidobacterium breve PRL2020 (Brevicillin®) treatment (Dietary Supplement)

结局指标

主要结局

Incidence of antibiotic-associated diarrhea (AAD)

时间窗: 7-10 days (according to antibiotic prescription)

Assessment of diarrhea occurring during antibiotic treatment with amoxicillin or amoxicillin/clavulanic acid. AAD will be counted starting from a single episode of diarrhea and not only after three or more episodes in one day, differing from the standard AAD definition.

Incidence of gastrointestinal symptoms other than diarrhea

时间窗: 7-10 days (according to antibiotic prescription)

Evaluation of gastrointestinal symptoms related to antibiotic therapy, including constipation, nausea, vomiting, abdominal cramps, bloating, and loss of appetite. These will be recorded daily by parents or legal guardians during the antibiotic course.

次要结局

  • Change in gut microbiota diversity following probiotic and antibiotic treatment(7-10 days (according to antibiotic prescription))
  • Tolerability of probiotic treatment(7-10 days (according to antibiotic prescription))
  • Adherence to probiotic treatment(7-10 days (according to antibiotic prescription))

研究者

发起方
Liaquat University of Medical & Health Sciences
申办方类型
Other
责任方
Principal Investigator
主要研究者

Dr. Amjad Khan

Professor

Liaquat University of Medical & Health Sciences

研究点 (1)

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