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临床试验/PACTR202102678743565
PACTR202102678743565尚未招募3 期

Pancreatic Enzymes and Bile Acids: A Non-Antibiotic approach to Treat Intestinal Dysbiosis in Acutely Ill Severely Malnourished Children (PB-SAM)

niversity of Oxford0 个研究点目标入组 1,200 人开始时间: 2021年1月20日最近更新:
适应症

试验速览

阶段
3 期
状态
尚未招募
入组人数
1,200

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
1 Month(s) 至 23 Month(s)(—)
性别
All

入选标准

  • Age =2 to <59 months
  • Admitted to hospital with an acute, non-traumatic illness and within 72 hours of admission at the time of enrolment
  • Severe malnutrition (weight-for-height <-3 z scores of the median WHO growth standards and/or mid upper arm circumference <115mm (<110mm age below 6 months), or symmetrical oedema of at least the feet related to malnutrition (not related to a primary cardiac or renal disorder)
  • Presence of two or more features of severity as specified in the protocol and trial SOP. If a child meets two criteria, they may be enrolled before further criteria are assessed (e.g. a child may be eligible on clinical signs before the complete blood count results are known).
  • Accompanied by care provider who provides written informed consent
  • Primary caregiver plans to stay in the study area during the duration of the study.

排除标准

  • Requires immediate cardiac/respiratory resuscitation (may be re-evaluated for study eligibility within 72h of admission)
  • Presence of terminal illness (other than severe acute malnutrition) likely to result in death within 6 months in the opinion of the recruitment team
  • Known congenital heart disease
  • Admission for traumatic or surgical indication
  • Known liver disorder or exocrine pancreatic disorder – e.g. biliary atresia, history of gallstones, cystic fibrosis or clinical jaundice
  • Known stomach or duodenal ulcer
  • Residence is outside the catchment area of study hospital
  • Primary caregiver declines to provide informed consent
  • Known intolerance or allergy to any study medication

研究者

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