Tokyo, Dec. 1 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000059409) titled 'Effect of Sage Juice Consumption on Mineral Absorption - 2nd trial' on Nov. 30.
Study Type:
Interventional
Study Design:
Basic Design - Cross-over
Randomization - Randomized
Blinding - Double blind -all involved are blinded
Control - Placebo
Primary Sponsor:
Institute - Finess Co, Ltd.
Condition:
Condition - Healthy Adults
Classification by malignancy - Others
Genomic information - NO
Objective:
Narrative objectives1 - A preliminary study will be conducted to confirm the effect of the test food, seabuckthorn Juice, on promoting the absorption of minerals from the diet.
Basic objectives2 - Efficacy
Intervention:
Interventions/Control_1 - seabuckthorn juice
Interventions/Control_2 - Placebo juice
Eligibility:
Age-lower limit - 20
years-old
=
Gender - Male and Female
Key inclusion criteria - (1) A person who does not suffer from any disease
(2) Males between the ages of 20 and 60
(3) BMI less than 30 kg/m2
(4) Persons who give written voluntary consent to participate in the study
(5) Who are able to drink seabuckthorn Juice on a continuous basis
Key exclusion criteria - (1) Those who are currently under medication for iron deficiency anemia
(2) Those who are currently receiving medication for some disease.
(3) Those who are consuming foods or health foods containing the active ingredients of the food under study.
(4) Persons with serious diseases or psychiatric disorders of glucose metabolism, lipid metabolism, liver function, renal function, heart, circulatory system, respiratory system, endocrine system, immune system, nervous system and those with a history of such diseases
(5) Persons with a history of abnormal laboratory values that would be considered problematic for study participation
(6) Persons who have a disease under treatment or a history of a serious disease that required medication
(7) Persons who may develop allergies related to the study
(8) Subjects who are judged to be unsuitable as subjects based on the results of the lifestyle questionnaire
(9) Subjects who are participating in other clinical studies at the time this study is initiated.
(10) Persons who are judged by the investigator (or study administrator) to be unsuitable to participate in the study.
Target Size - 20
Recruitment Status:
Recruitment status - Preinitiation
Date of protocol fixation - 2025 Year 08 Month 30 Day
Anticipated trial start date - 2025 Year 10 Month 21 Day
Last follow-up date - 2025 Year 12 Month 30 Day
To know more, visit https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000067945
Disclaimer: Curated by HT Syndication.
