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临床试验/NL-OMON46407
NL-OMON46407已完成不适用

icorice Influences on cortisol/cortisone, electrolytes and blood pressure - LICORICE study

Academisch Medisch Centrum0 个研究点目标入组 40 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
40

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 至 99(—)

入选标准

  • - Willing and able to participate in the study protocol
  • - Written informed consent
  • - Age 18-60 years
  • - Office diastolic blood pressure maximal 90 mmHg and office systolic blood pressure maximal 140 mmHg
  • - BMI > 18 or < 35 g/m2
  • - No use of medication which affects the primary or secondary outcome measurements such as diuretics, antihypertensive drugs and NSAIDs < six weeks before start of the study
  • - Willing to adhere to the study protocol
  • - Accessible veins on arm(s) as determined by examination at information meetings

排除标准

  • - Allergy to one of the ingredients of licorice
  • - Office blood pressure >140/90 mm
  • - Reported alcohol consumption > 28 units/week or recreational drug use
  • - Existing cardiovascular diseases
  • - Use of medication which affects the primary or secondary outcome measurements such as diuretics, antihypertensive drugs and NSAIDs < six weeks before start of the study
  • - Currently on a medically prescribed diet, or slimming diet
  • - Potassium <3.5 mmol/l
  • - eGFR <60
  • - Excessive ingestion of licorice (>200 gr/week) or >3 litre of licorice tea per week
  • - Pregnancy

研究者

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