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临床试验/NL-OMON34781
NL-OMON34781已完成不适用

BIOEQUIVALENCE STUDY 2010 Comparison of the absorption of MK-7 after intake of 3 different existing MK-7 supplements - BIOEQUIVALENCE STUDY 2010

niversiteit Maastricht0 个研究点目标入组 24 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
已完成
入组人数
24

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 99(—)

入选标准

  • * Healthy men and women, aged between 20 and 40 years
  • * Normal body weight and height (18.5 kg/m2 < BMI <30 kg/m2)
  • * Stable body weight (weight gain or loss <3 kg in past 3 mo)
  • * Written consent to take part in the study
  • * Agreement to adhere to dietary restrictions required by the protocol

排除标准

  • * Abuse of drugs and/or alcohol
  • * Use of vitamin supplements containing vitamin K
  • * Soy allergy
  • * Pregnancy
  • * (a history of) metabolic or gastrointestinal diseases including hepatic disorders
  • * Chronic degenerative and/or inflammatory diseases, e.g. diabetes mellitus, renal failure
  • * Use of oral anticoagulants
  • * Corticoid treatment
  • * Subjects with anaemia or subjects who recently donated blood or plasma
  • * Systemic treatment or topical treatment likely to interfere with coagulation metabolism (salicylates, antibiotics)
  • * Chronic degenerative and/or inflammatory diseases
  • * Use of oral anticoagulants
  • * Corticoid treatment
  • * Systemic treatment or topical treatment likely to interfere with evaluation of the study parameters

研究者

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