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临床试验/JPRN-UMIN000016456
JPRN-UMIN000016456尚未招募未知

A clinical study for evaluating the efficacy and safety of long-term consumption of the honey vinegar beverage on lowering blood pressure in the subjects with high normal blood pressure or grade 1 hypertension - A clinical study for evaluating the efficacy and safety of long-term consumption of the honey vinegar beverage on lowering blood pressure

Soiken Inc.0 个研究点目标入组 100 人开始时间: 2016年8月31日最近更新:
适应症

试验速览

阶段
未知
状态
尚未招募
发起方
Soiken Inc.
入组人数
100

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
20years-old 至 65years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1) Subjects who need an urgent anti-hypertensive treatment 2) Subjects who have a symptom of cerebrovascular diseases 3) Heart failure patients or subjects who have a history of myocardial infarction 4) Subjects who have an atrial fibrillation or a severe arrhythmia 5) Subjects who have a severe renal dysfunction (serum creatinine >=2 mg/dl) 6) Subjects who have severe hepatic, cardiovascular, respiratory disease, endocrine or metabolic disorders 7) Subjects who have a history of the hypersensitivity or an allergy for test foods in this study 8) Subjects who have a secondary hypertension 9) Subjects who regularly take any anti-hypertensive drug or FOSHU for improving hypertension 10) For female: Subjects with pregnant or breast feeding , or those who have a plan to be pregnant during the study period 11) Subject having blood sample of 200 ml or more taken (e.g., donated blood) within 1 month, or 400 ml or more within 3 months prior to the start of the present study 12) Subject who took part in another clinical study within 3 months prior to the start of the present study or who is currently taking part in another clinical study 13) Subject deemed unsuitable by the investigator

研究者

发起方
Soiken Inc.

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