Evaluation of the Effectiveness of Treatment With Bifidobacteria in Children Affected by Seasonal Allergic Rhinitis
试验速览
- 阶段
- 3 期
- 入组人数
- 40
- 试验地点
- 1
- 主要终点
- Evaluation of the symptoms by structural questionary
研究概览
简要总结
This study is aimed at assessing the efficacy of supplementation with a mixture of three bifidobacteria , on the allergic rhinitis..The rhinitis symptoms were assessed by validated score ( TSS ) , for children aged between 4 and 17 years with allergic rhinitis parietaria , mild , moderate or severe , than children not supplemented .
Secondary Objectives
- The effectiveness of treatment by VAS :
- Evaluation of the rescue medication consumption
- Evaluation of quality of life ( using structured questionnaire )
- Evaluation of the frequency and school performance ( using structured questionnaire )
- Assessment of sleep quality and attention (through structured questionnaire )
- Satisfaction rating and satisfaction of parents
- Evaluation of asthma exacerbations in children susceptible
详细描述
This is a randomized , double-blind , placebo - controlled , phase 3 , 2 arms , in which patients were selected to receive placebo or a mixture powder composed of three bifidobacteria : Bifidobacterium Longum BB536 ( 3 billion units ) + Bifidobacterium infantis M - 63 ( 1 billion units ) Bifidobacterium breve M + -16 V ( 1 billion units ) . The subjects included in our study are represented by children aged between 4 and 17 years , with seasonal allergic rhinitis moderate and presenting positive skin prick test against parietaria.The participation of each subject in the study was based on evaluation of its clinical history. The recruited patients were divided into two groups according to the drug used.The group A received placebo , while the group B mixture bifidobacteria. The treatment was performed for a period of two months. At the beginning and at the end of therapy several surveys have been carried out , so as to be able to compare results and to draw some preliminary conclusions about the effectiveness of treatment.
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
- 4 Years 至 17 Years（Child）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Children of both sexes , aged from 4 to 17 years
- •History seasonal allergic rhinitis mild , moderate or severe , according to the guidelines defined AIR 2013 , documented by recurrent episodes in the previous year and confirmed by skin prick test positive
- •Written informed consent of one parent or a legal representative
排除标准
- •Lack of written informed consent by at least one parent or a legal representative
- •Concurrent disorders such as infection of the upper or lower respiratory tract , nasal surgery in the past year , respiratory tract abnormalities , immune diseases
- •Use of antihistamines , nasal or systemic corticosteroids , leukotriene modifiers , or cromolyn sodium , on an ongoing basis used in the last six weeks.
研究组 & 干预措施
Bifidobacteria mixture 0.5 ml
Bifidobacteria 0.5 ml per os all days for 2 months
干预措施: Bifidobacteria (Drug)
placebo
Placebo 0.5 ml per os all days for 2 months
干预措施: placebo (Drug)
结局指标
主要结局
Evaluation of the symptoms by structural questionary
时间窗: 2 months
次要结局
未报告次要终点
研究者
Prof. Michele Miraglia del Giudice
Prof. Associato
University of Campania "Luigi Vanvitelli"