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临床试验/PACTR201311000711179
PACTR201311000711179已完成未知

Enterosorbent Intervention Therapies for Populations at risk of Aflatoxin-Related Diseases: Safety evaluation of Unifrom Particle NovaSil in Children (Phase I)

oguchi Memorial Institute for Medical Research0 个研究点目标入组 75 人开始时间: 2013年11月22日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
75

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
3 Year(s) 至 9 Year(s)(—)
性别
All

入选标准

  • 1)Healthy (based on physical examinations)
  • 2)No history of chronic illness
  • 3)No use of prescribed medications for chronic or acute illness
  • 4)Normal urinalysis (protein, glucose and bilirubin) using chemstrip
  • 5)Normal hemoglobin level (greater than 10g/dl)
  • 6)The parent or guardian must sign or thumb print the consent form.

排除标准

  • 1)Those not meeting the inclusion criteria
  • 2)Abnormal hemoglobin level (below 10g/dl).

研究者

发起方
oguchi Memorial Institute for Medical Research

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Safety evaluation of Uniform Particle NovaSil in... | 临床试验