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临床试验/JPRN-jRCTs031230290
JPRN-jRCTs031230290招募中Unknown

Effect of synbiotics on uremic toxins in hemodialysis patients - before-after study

Goda Tomohito0 个研究点目标入组 40 人开始时间: 2023年8月14日最近更新:
适应症

试验速览

阶段
Unknown
状态
招募中
发起方
入组人数
40

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
>= 18age old 至 ot applicable(—)
性别
All

入选标准

  • 1) Maintenance hemodialysis patients who are outpatients at the time of informed consent
  • 2) Patients who introduced hemodialysis more than 6 months after consent was obtained
  • 3) Patients who can self-medicate
  • 4) Patients who are 18 years of age or older, have the ability to consent, and are able to obtain written consent of their own free will.

排除标准

  • 1) Patients with dementia
  • 2) Patients with inflammatory bowel disease, history of lower gastrointestinal surgery, marked ascites due to liver disease, active malignant tumor
  • 3) Patients who cannot stop taking other probiotics and synbiotic preparations, including supplements, from 2 weeks before the start of study drug administration until the end of the study
  • 4) Patients who cannot stop taking Lubiprostone, Linaclotide, and Elobixibat and general antiflatulent drugs from 2 weeks before the start of study drug administration until the end of the study
  • 5) Patients taking many sleeping pills
  • 6) Patients who are allergic to potatoes, corn, Lactobacillus/Bifidobacterium beverages/foods, and dairy products
  • 7) Women who are pregnant, may become pregnant, or are breastfeeding
  • 8) Patients with other conditions that the investigators judge to be inappropriate for the study

研究者

发起方
Goda Tomohito

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