MedPath

A study for evaluating the effect of the intake of a kale-containing green juice on blood pressure in adult males and females with a higher blood pressure.

Not Applicable
Conditions
healthy adult with a higher blood pressure
Registration Number
JPRN-UMIN000031450
Lead Sponsor
TTC Co., Ltd.
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
80
Inclusion Criteria

Not provided

Exclusion Criteria

(1) Subjects who routinely use green juice more than once per week (2) Subjects taking medicine, health food (including food for specified health use) and supplements which may influence blood pressure. (3) Subjects who have an allergy to plants of Brassicaceae including kale and metal, and may induce an allergy by participating in this study. (4) Subjects who have a disease under treatment (except hay fever sufferer without treatment during this study period and subjects with asthenopia only using eye drops). (5) Subjects who have under treatment or a history of serious disease (e.g., diabetes, liver disease, kidney disease, or heart disease) (6) Subjects taking warfarin potassium (vitamin k-dependent coagulation factor synthesis inhibitors). (7) Subjects who are judged as unsuitable for the study based on the results of clinical and physical examination on preliminary examination. (8) Subjects who have participated in other clinical study within the last one month prior to the current study or are planned to participate in other clinical study after informed consent for the current study. (9) Subjects who can not keep restriction and prohibited matter during this study period. (10) Subjects who have habits affecting research results, such as doing shift work day and night, or Subjects who have a plan that affect research results such as day and night shift work and overseas. (11) Subjects who are planned to become pregnant after informed consent for the current study or are pregnant or lactating. (12)Subjects who are judged as unsuitable for the study based on the results of lifestyle questionnaire. (13)Subjects who are judged as unsuitable for the study by the investigator for other reason.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Systolic blood pressure, diastolic pressure
Secondary Outcome Measures
NameTimeMethod
© Copyright 2025. All Rights Reserved by MedPath