Efficacy trial of 4 weeks ingestion of the development code MSHF001 food

Not Applicable

• Conditions: Healthy adults

• Registration Number: JPRN-UMIN000038871
• Lead Sponsor: Kao Corporation

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2019-12-13
• Study Completion: 2020-04-14
• Last Update Posted: 17 October 2023

Recruitment & Eligibility

• Status: Complete: follow-up complete
• Sex: Female
• Target Recruitment: 100

Inclusion Criteria

Not provided

Exclusion Criteria

-Subjects with systemic illness. -Subjects who are diagnosed as menopausal disorders. -Subjects who are under Hormone Replacement Therapy, HRT, and/or medication which would affect blood hormone levels. -Subjects who are outpatients or were treated by doctor within a month. -Subjects who regularly take medicine. -Subjects who regularly take medicines that affect menopausal symptoms. -Subjects who are pregnant or lactating, or planned to become pregnant in the near future. -Subjects with smoking habit. -Subjects with drinking habit in 5 or more days a week. -Subjects who have possibilities for emerging allergy to foods, metals, and drugs. -Subjects with illnesses or diseases on their face, especially such as atopic dermatitis, or psoriasis, or severe acne. -Subjects who habitually having specific polyphenol-rich health food and drink. -Subjects with high anxiety questionnaire values. -Subjects with high Kupperman Kohnenki Shohgai Index. -Subjects who easily have skin rashes. -Subjects with potential conflict of interest.

Study & Design

• Study Type: Interventional
• Study Design: Not specified