Tokyo, July 22 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000058536) titled 'The eff ect of test food (FF16) for skin in healthy adults' on July 22.
Study Type:
Interventional
Study Design:
Basic Design - Cross-over
Randomization - Randomized
Blinding - Double blind -all involved are blinded
Control - Placebo
Primary Sponsor:
Institute - KOEI SCIENCE LABORATORY Co., Ltd.
Condition:
Condition - NO
Classification by malignancy - Others
Genomic information - NO
Objective:
Narrative objectives1 - This study aims to examine effects of a test food for skin conditions and its Safety for responder group.
Basic objectives2 - Safety,Efficacy
Intervention:
Interventions/Control_1 - Oral intake of the test product (1 pack a day,4weeks(pre-test), 8weeks(main-test)).
Interventions/Control_2 - Oral intake of the placebo product (1 pack a day,4weeks(pre-test), 8weeks(main-test)).
Eligibility:
Age-lower limit - 20
years-old
=
Gender - Male and Female
Key inclusion criteria - (1) from 20years old to 70years old.
(2) Individuals whose written informed consent has been obtained after explanation of this study.
Key exclusion criteria - (1) patient
(2) individuals who are sensitive to test product or other foods, and medical products.
(3) individuals judged inappropriate for the study by the principal.
Target Size - 40
Recruitment Status:
Recruitment status - Completed
Date of protocol fixation - 2023 Year 12 Month 01 Day
Date of IRB - 2023 Year 12 Month 23 Day
Anticipated trial start date - 2024 Year 01 Month 06 Day
Last follow-up date - 2024 Year 11 Month 30 Day
To know more, visit https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000066935
Disclaimer: Curated by HT Syndication.
