跳至主要内容
临床试验/NCT00937274
NCT00937274终止不适用

Randomized, Double Blind Placebo-controlled Studies to Evaluate the Effect of an Orally-fed Escherichia Coli (E. Coli) Phage in the Management of ETEC and EPEC Induced Diarrhea in Children

Société des Produits Nestlé (SPN)1 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2009年8月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
终止
发起方
入组人数
120
试验地点
1
主要终点
Assessment of safety, tolerability and efficacy (reduce severity of diarrhea assessed by reduced stool volume and stool frequency) of oral administration of T4 phages in young children with diarrhea due to ETEC and/or EPEC infections

研究概览

简要总结

This study hopes to demonstrate the potentials of a new form of therapy for childhood diarrhea, a major cause of morbidity and deaths in Bangladesh and other developing countries, and thus a priority for improving child health.

详细描述

This randomized double-blind, placebo controlled trial (RCT) aims to evaluate the effect of oral administered E. coli phage in children aged 4-60 months of age with proven ETEC and EPEC diarrhea. Children will be screened to exclude V. cholerae infections by dark field microscopy, rotavirus by stool ELISA, and invasive diarrhoea clinically as well as by stool microscopy, to identify children with possible ETEC and EPEC diarrhoea. Enrolled children will be randomly assigned, in equal numbers, to receive either: (i) a new T4 phage cocktail or (ii) Russian anti-E. coli phage cocktail (Microgen) at the dose recommended by the manufacturer or (iii) only oral rehydration solution (placebo) for 5 days in addition to management of dehydration and continued feeding in accordance with WHO guidelines. Duration of diarrhea, daily and cumulative stool output, volume of oral rehydration solution intake, stool frequency, time to recovery and weight gain will be the main outcome measures. As the dose of phage we intend to use in this therapeutic trial is higher than the dose administered to young children in earlier safety trial, we plan to initially conduct a safety study with these three study products in 45 children with non cholera, non rotavirus and non invasive diarrhea, to randomize equally in the three intervention groups, as for the final study mentioned above. The outcome measures in this safety part will include assessment of laboratory parameters including renal and liver function tests, haematological indices, and microbiological efficacy of phage by measuring phage and E. coli titre in daily stool samples. If the higher dose is found safe, tolerable, and not associated with any significant adverse event, we will proceed to the clinical efficacy trial.

We believe if T4 coli phage is assessed to be effective in the overall diarrhea management, this might lead to development of an affordable and sustainable adjunct to the currently available case management of E. coli diarrhea, benefiting millions of children worldwide.

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
6 Months 至 24 Months(Child)
性别
Male
接受健康志愿者
否

入选标准

  • •Age: 6 - 24 months
  • •Better nourished (weight for age > 60 NCHS median)
  • •H/o. diarrhea of less than 48 hours
  • •Written informed consent from either parents/guardian (thumb impression for those who are not literate) for children
  • •Negative test results for dark field microscopy of Vibrio cholerae and ELISA test for rotavirus in initial stool samples

排除标准

  • •Systemic infection requiring antibiotic treatment
  • •Severe malnutrition (W/A < 60%)
  • •Unwilling to comply with study procedures
  • •Currently participating or have participated in another clinical trial within the last 4 weeks at screening
  • •Clinically significant abnormalities from medical history, physical examination, vital signs, haematology, clinical chemistry results, or other laboratory abnormalities
  • •Clinically suggestive of invasive diarrhea

研究组 & 干预措施

Standard care

Placebo Comparator

干预措施: standard oral rehydration solution (ORS) (Other)

Test product

Experimental

干预措施: T4 phage cocktail test (Other)

Commercial product

Active Comparator

干预措施: Commercial T4 phage cocktail (Other)

结局指标

主要结局

Assessment of safety, tolerability and efficacy (reduce severity of diarrhea assessed by reduced stool volume and stool frequency) of oral administration of T4 phages in young children with diarrhea due to ETEC and/or EPEC infections

时间窗: 5 days

次要结局

  • Clinical assessment, blood tests, morbidity, duration of hospitalization(5 days)

研究者

发起方
Société des Produits Nestlé (SPN)
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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