Effects of Single Ingestion of Hydrogen Water (Generated through Hydrogen Water Server) on Blood Flow: A Randomized, Double-blind, Placebo-Controlled, Cross-Over Trial

Not Applicable

• Conditions: /A (healthy adults or adults being sensitive to the cold)

• Registration Number: JPRN-UMIN000023963
• Lead Sponsor: TES Holdings Co., Ltd.

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2016-09-10
• Last Update Posted: 17 October 2023

Recruitment & Eligibility

• Status: Complete: follow-up complete
• Sex: Female
• Target Recruitment: 30

Inclusion Criteria

Not provided

Exclusion Criteria

[1]Individuals using medical products [2]Individuals who are patient or have a history of psychiatric disease, high blood pressure, diabetes, and hyperlipidemia [3]Individuals who used a drug to treat a disease in the past 1 month (except temporal usage for pollenosis) [4]Individuals who conducted hormone replacement therapy in the past 3 months or have a history of conducting hormone replacement therapy [5]Individuals who have a history of serious hepatopathy, kidney damage, heart disease and hematological disease [6]Individuals who are a patient or have a history of or endocrine disease [7]Individuals with serious anemia [8]Individuals who are sensitive to a test product or other foods, and medical products [9]Individuals who have a habit to intake hydrogen water [10]Individuals who had a habit to ingest health-promoting foods, foods for specified health uses, health foods, or supplyments in the past 3 months or will ingest those foods during the test period [11]Individuals who have an inflammation or a scar on a measuring area [12]Individuals whose BMI is over 25 [13]Individuals whose systolic blood pressure is over 160mmHg or diastolic pressure is over 100mmHg [14]Individuals who excessively take alcohol (expressed in an amount of alcohol: over 60mg/day) [15]Individuals who are a smoker [16]Individuals who participated in other clinical studies in the past 3 months [17]Individuals whose SMI score is over 66 [18]Individuals who have a history of ovarian resection or hysterectomy [19]Individuals who are or are posslibly, or are lactating [20]Individuals judged inappropriate for the study by the principal

Study & Design

• Study Type: Interventional
• Study Design: Not specified