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临床试验/NCT03078842
NCT03078842已完成不适用

Establishing the Optimal Dose of Therapeutic Zinc Supplementation for the Treatment of Acute Diarrhea in Under Five Children - a Dose Response Trial in a South Asian and a Sub-Saharan African Setting

Ayesha De Costa2 个研究点 分布在 2 个国家目标入组 4,500 人开始时间: 2017年1月23日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
4,500
试验地点
2
主要终点
Proportion with long duration of diarrhoea

研究概览

简要总结

Diarrhoea continues to be a major cause of child deaths. Current treatment of acute watery diarrhoea includes oral rehydration solution (ORS), zinc and continued feeding. The use of zinc is based on a number of studies that showed that zinc reduces the duration and severity of diarrhoea. The recommended dose of zinc in 6-59 month old children is 20mg/day for 10-14 days. This dose is associated with an increased risk of vomiting. No dosing studies are available to determine the optimal dose of zinc, which while maintaining the benefits also has a low risk of vomiting.

The investigators will conduct a double-blind randomized controlled trial of three doses of zinc (20mg/day, 10mg/day and 5mg/day) in two settings - one in Sub-Saharan Africa and the other in South Asia. The study population will be 4500 children with diarrhoea of less than 72 hours duration who are aged 6-59 months. They will be recruited from outpatient health facilities. All enrolled children will receive ORS and continued feeding as recommended by the World Health Organization. Those allocated to the standard zinc dose will receive an oral dispersible tablet with 20mg zinc daily for 14 days. Those allocated to lower dose zinc will receive identical tablets with either 10mg or 5mg zinc daily for 14 days. Enrolled children will be followed by until recovery from diarrhoea or 15 days after enrolment, whichever is later. In addition, study children will be assessed again at thirty (30), forty-five (45), and sixty (60) days to estimate impact on post illness outcomes. Primary outcomes will be mean duration of diarrhoea, proportion of episodes that last longer than 5 days, mean number of stools and proportion of children with vomiting.

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)

盲法说明

All participants will get dispersible zinc tablets that, contain either 20 mg, 10 mg, or 5 mg of zinc. All tablets look and taste the same. Randomization and tablet package labelling was done in Geneva, and no-one at the trial sites knows the actual zinc content of tablets packaged for each participant number.

入排标准

年龄范围
6 Months 至 59 Months(Child)
性别
All
接受健康志愿者

入选标准

  • 6 to 59 completed months of age
  • Acute diarrhoea of less than 3 days at the time of screening or dysentery, defined as visible blood in the stool, of less than 3 days at the time of screening
  • Likely to stay within the study area for the next 2 months
  • Written informed consent from caretaker

排除标准

  • Presence of severe acute malnutrition (WHZ<-3 or oedema)
  • Presence of severe dehydration that cannot be corrected in 4 to 6 hours
  • Signs of severe pneumonia (WHO definition of pneumonia with danger signs), sepsis, rapid diagnostic test (RDT) -confirmed malaria or other severe illness
  • Previously or currently enrolled in the study
  • Currently enrolled in another study
  • Other child currently enrolled in the study in the same household
  • Not intending to remain in study area for the duration of the study
  • Parents refuse participation in the study

结局指标

主要结局

Proportion with long duration of diarrhoea

时间窗: Measured daily for 15 days

Diarrhoea continuing beyond five days

Continuation of diarrhoea symptoms

时间窗: Measured daily for 15 days

Total number of loose or watery stools after enrolment

Proportion of children vomiting after zinc treatment

时间窗: Measured daily for 15 days

Vomiting within 30 minutes of administration of zinc tablet

次要结局

  • Proportion with intermediate duration of diarrhoea(Measured daily for 15 days)
  • Treatment adherence(Measured daily for 15 days)
  • Proportion of children experiencing serious adverse events (SAEs)(Measured until 60 days)
  • Proportion of guardians with positive attitude towards treatment(Day 15)
  • Illness symptoms between day 15 and 60 after the treatment(Days 30, 45, 60)
  • Mean serum plasma zinc concentration at Days 1, 3, 7, 15, 21 and 30(Days 1, 3, 7, 15, 21 and 30)

研究者

发起方
Ayesha De Costa
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Ayesha De Costa

Scientist

World Health Organization

研究点 (2)

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