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临床试验/JPRN-UMIN000001329
JPRN-UMIN000001329已完成2 期

A Randomized trial to assess the effects of hydrogen-rich dissolution water for patients with impaired glucose tolerance or impaired fasting glucose

Kyoto Prefectural University of medicine0 个研究点目标入组 60 人开始时间: 2008年8月21日最近更新:

试验速览

阶段
2 期
状态
已完成
入组人数
60

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
20years-old 至 70years-old(—)
性别
All

入选标准

  • 1) Patients who are abele to give written informed consent
  • 2) FBS is over 100mg/dl and under 126mg/dl in registration
  • 3) Age is over 20 years and less than 80 years
  • 4) Type of practice: outpatient department
  • 5) Patients are able to do the following things in this trial - getting good compliance with consuming investigational food and coming to hospital, and writing the diary and the questionnaire accurately by themselves

排除标准

  • 1) Patients who have receive drug treatment for diabetes
  • 2) Patients with the diseases which have possibility with impaired glucose tolerance
  • 3) Patients with serious liver or kidney damage
  • 4) Patients with serious heart disease or cerebrovascular disorders
  • 5) Patients with serious disease in pancreas or blood disease
  • 6) Patients with malignant tumors which effect their general status or survival time
  • 7) Patients who are in pregnancy, while breast-feeding, have possibilities of them, or desire pregnancy in test period
  • 8) Patients with alcohol abuse
  • 9) Patients who have taken part in the her clinical research within 12 weeks
  • 10) Patients who have taken part in the her clinical research within 12 weeks
  • 11) Patients who are inadequate, which their physicians assessed it

研究者

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