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临床试验/NL-OMON56610
NL-OMON56610撤回不适用

Randomized placebo-controlled pilot study to determine the effect of probiotics on vitamin K status in renal transplant recipients - Probiotics and vitamin K2 status

niversitair Medisch Centrum Groningen0 个研究点目标入组 20 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
撤回
入组人数
20

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
18 至 64(—)

入选标准

  • 1. Adult renal transplant recipient >1 year post transplantation
  • 2. Signed informed consent

排除标准

  • 1. Renal transplant recipient <1 year post transplantation
  • 2. Consuming probiotic supplements in the past 3 months
  • 3. Patients receiving any form of antibiotic treatment in the past 3 months
  • 4. Any supplementation of Vitamin K (e.g. multivitamin)
  • 5. Medical history of blood clotting disorders (hypercoagulable states) and
  • increased risk of thrombosis (history of myocardial infarction, percutaneous
  • transluminal angioplasty/stenting of coronary of peripheral arteries, bypass
  • operation, intermittent claudication, amputation for vascular reasons,
  • transient ischemic attack (TIA) or ischemic cerebrovascular accident).
  • 6. Gastrointestinal disorders or undergone digestive tract surgery (except
  • appendectomy)
  • 7. Use of medication that would interfere with the study parameters: Vitamin K
  • antagonists or fytomenadion
  • 8. Reported slimming or medically prescribed diet
  • 9. Pregnancy, lactation or a female planning to conceive within the study
  • period (a pregnancy test will be performed if there is any doubt regarding a
  • potential pregnancy).

研究者

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