跳至主要内容
临床试验/NL-OMON51421
NL-OMON51421已完成不适用

Antioxidant and immune effects of vitamin K2 - ProteK2t study

Kappa Bioscience AS0 个研究点目标入组 60 人开始时间: 待定最近更新:

试验速览

阶段
不适用
状态
已完成
发起方
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
18 至 99(—)

入选标准

  • Age >=50 and <=75;
  • Self-reported postmenopausal (at least one year after the final menstruation)
  • BMI >=25 and <=32 kg/m2;
  • Plasma dp-ucMGP concentration in highest 50-66% of the screened population
  • Non-smoking (defined as not smoking currently and not having smoked (at all)
  • in the year before study start);;
  • Healthy as assessed by health questionnaire (*Gezondheidsvragenlijst*) and
  • according to the judgment of the study physician;
  • Voluntary participation;
  • Having given written informed consent;
  • Willing to comply with study procedures;
  • Accept use of all encoded data, including publication, and the confidential
  • use and storage of all data for 15 years;

排除标准

  • Plasma dp-ucMGP concentration >1000 pmol/L at screening
  • Treatment with oral antibiotics within 2 months of the start of the study
  • Any vaccination in the month before study start or any scheduled vaccination
  • during the study period
  • Use of antioxidant or vitamin K and D supplements;
  • Use of antioxidant or vitamin K and D supplements in the 3 months before the
  • start of the study;
  • Use of aspirin or medication with established antioxidant or
  • anti-inflammatory properties;
  • Use of medication that interferes with vitamin K or blood coagulation;
  • Use of statins to reduce level of low-density lipoprotein cholesterol in the
  • Hyperlipidaemia, diabetes, hypertension, intestinal disease, diseases with an
  • inflammation component;
  • Hormone replacement therapy in women;
  • Follow a vegetarian or vegan diet;
  • Participation in any clinical trial including blood sampling and/or
  • administration of substances up to 30 days before day 1 of this study;
  • Alcohol consumption for men > 28 units/week and >4/day; for women: >21
  • units/week and >3/day;
  • Reported unexpected weight loss or weight gain of > 3 kg in the month prior
  • to pre-study screening, or intention to lose weight during the study period;
  • Reported slimming or medically prescribed diet;
  • Recent blood donation (<1 month prior to Day 01 of the study);
  • Not willing to give up blood donation during the study;
  • Personnel of NIZO food research, EB Medical Research and Kappa Bioscience,
  • their partner and their first and second degree relatives;
  • Not having a general practitioner;
  • Not willing to accept information-transfer concerning participation in the
  • study, or information regarding his or her health, like laboratory results and
  • eventual adverse events to and from his general practitioner

研究者

发起方
Kappa Bioscience AS

相似试验