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临床试验/NCT00457353
NCT00457353已完成3 期

Phase III Comparative Study to Assess the Efficacy and Safety of Oral Rehydration Therapy (ORT) in Combination With Spores of Bacillus Clausii (Enterogermina)Versus ORT Alone, Administered for 5 Days With the Treatment of Acute Diarrhea in Children.

Sanofi1 个研究点 分布在 1 个国家目标入组 264 人开始时间: 2007年3月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
发起方
Sanofi
入组人数
264
试验地点
1
主要终点
Reduction in duration of diarrhea

研究概览

简要总结

Primary:

  • To demonstrate the efficacy of Enterogermina® in reducing the duration of acute diarrhea in children

Secondary:

  • To evaluate the safety of Enterogermina® in acute diarrhea in Indian children

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
6 Months 至 5 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Non hospitalised infants and children attending clinic/outpatients with acute diarrhea (>3 liquid or watery stools occurring in a 24-hour period) of less than 48 hours duration

排除标准

  • History of presence of blood, pus, or mucus in stools
  • Severe dehydration (World Health Organization criteria)
  • Severely malnourished patients
  • Treatment with antibiotics, probiotics, or prebiotics within a period of 2 weeks before enrolment
  • History of conditions known to producing immunodeficiency (Acquired Immune Deficiency Syndrome, other congenital immunodeficiency syndrome, drug therapy with steroids, anticancer drugs etc)
  • Known hypersensitivity to Bacillus clausii or other probiotics.
  • The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.

研究组 & 干预措施

1

Active Comparator

Administration of oral rehydration therapy with Bacillus clausii probiotic strain (1 vial twice daily, each vial containing 2 billion spores of Bacillus clausii)

干预措施: Bacillus Clausii (Drug)

2

Placebo Comparator

Administration of Oral rehydration therapy

干预措施: Oral rehydration therapy (Other)

结局指标

主要结局

Reduction in duration of diarrhea

时间窗: Throughout the treatment period

Incidence of adverse events

时间窗: Throughout the study period

次要结局

  • Mean number of stools per day(Throughout the treatment period)
  • Effect on consistency of stools(Throughtout the treatment period)
  • Vomiting episodes per day(Throughout the treatment period)
  • Requirement of unscheduled intravenous transfusion(Throughout the study period)
  • Need for hospitalization(Throughout the treatment period)

研究者

发起方
Sanofi
申办方类型
Industry

研究点 (1)

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