Study on effects of Luffa cylindrica intake by different cooking methods on blood pressure

Not Applicable

Recruiting

• Conditions: Subjects with high normal blood pressure or grade 1 hypertension

• Registration Number: JPRN-UMIN000038270
• Lead Sponsor: nicersity of the Ryukyus

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2019-10-11
• Study Completion: 2021-05-31
• Last Update Posted: 17 October 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 180

Inclusion Criteria

Not provided

Exclusion Criteria

1) Subjects who regularly consume medicines, food for specified health use, health food, etc. that may affect the test results. 2) Subjects who are currently on a diet or are planning a diet. 3) Subjects who plan to travel for a long time during the examination period. 4) Alcoholic drinkers (Alcohol intake 60 g / day or more). 5) Subjects who have irregular diets, irregular shift rhythms, shift workers, late-night workers. 6) Subjects who have a history of serious diseases such as heart, liver, kidney, digestive system etc. 7) Subjects who are pregnant, planning pregnancy or nursing. 8) Subjects who are participating in clinical trials of other medicines or health food, within 4 weeks after the end of the trial, or who are planning to participate in other clinical trials after consenting to participate in the trial. 9) Subjects who are continuing treatment with drugs. 10) Subjects who are allergic to medicines or food (especially Luffa). 11) Subjects who performed component blood donation or blood donation of 200mL of whole blood from the month before the start of the trial. 12) Men who performed blood donation of 400mL whole blood three months before the start of the trail. 13) Women who performed blood donation of 400mL whole blood four months before the start of the trial. 14) Subjects who was judged by the study principal physician or the trial division physician to be inappropriate to participate in this trial.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
homoe blood pressure (Systolic blood pressure and Diatolic blood pressure)

Secondary Outcome Measures

Name	Time	Method
blood pressure, heart rate, body weight, urinary sodium and pottasium, defecation status