跳至主要内容
临床试验/CTRI/2017/02/007966
CTRI/2017/02/007966已完成3 期

Zinc as an adjunct for the treatment of clinical severe infection in infants younger than 2 months

Translational Health Science and Technology Institute0 个研究点目标入组 2,913 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
2,913

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

入选标准

  • We have adapted the inclusion criteria from the WHO IMCI and IMNCI to identify very sick infants aged 3 days to 59 days with clinical severe infection
  • 1)Low body temperature less than 35.5 deg Celsius AND, OR
  • 2)Movement only when stimulated AND, OR
  • 3)Stopped feeding well AND, OR
  • 4)Severe chest indrawing AND, OR
  • 5) Axillary temperature more than or equal to 38.0 deg Celsius and Infant should have been well at some point from birth till the current episode of illness

排除标准

  • 1) Surgical or life-threatening malformation or condition that will interfere with administration of oral or oro-gastric (OG) or naso-gastric (NG) intervention
  • 2) Infants requiring surgical intervention or admission outside of pediatric ward for management
  • 3) Documented evidence of having received more than 1mg of elemental zinc per day in the last 48 hours
  • 4) Documented evidence of having received injectable antibiotics for 48 hours or more for this illness episode
  • 5) Weight at presentation less than 1500 gm
  • 6) infants requiring exchange transfusion
  • Those infants who fulfill the criteria of clinical severe infection and do not have any exclusion criteria but are very sick and not allowed oral or nasogastric intervention will not be enrolled immediately but will be observed during a stabilization period when they will be observed by the study nurse every 8th hourly for a maximum period of 24 hours of
  • stabilization. Infants who have been stabilized and allowed orally, anytime within the 24 hour stabilization period and who after stabilization continue to have at least one sign of clinical severe infection, no exclusion criteria and whose parents or guardians have given written informed consent for participation will now fulfill the eligibility criteria

研究者

发起方
Translational Health Science and Technology Institute

相似试验