A study of the effect of improving urinary problems with foods containing Brazilian green propolis extract, pumpkin seed extract and cranberry extract in healthy wome

Not Applicable

• Conditions: Adult

• Registration Number: JPRN-UMIN000046228
• Lead Sponsor: Yamada Bee Company, Inc.

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2021-11-30
• Study Completion: 2022-03-31
• Last Update Posted: 17 October 2023

Recruitment & Eligibility

• Status: Complete: follow-up complete
• Sex: Female
• Target Recruitment: 84

Inclusion Criteria

Not provided

Exclusion Criteria

1. Individuals who undergoing treatment for urinary disorders such as overactive bladder, bladder inflammation, and urethral stones. 2. Individuals whose OABSS score is over 2 point in the Q. 3 and over 3 points in the total score of the OABSS. 3. Individuals with a current history of diabetes, cerebrovascular accidents, sequelae of stroke, spinal cord disorders, spinal degenerative disorders, sleep disorders, mental disorder and hypertension. 4. Individuals who have a disorder to absorption, distribution, metabolism, excretion of food, such as digestive tract, liver, kidney, heart and cardiovascular system. 5. Individuals with a history of the surgery considerable in the gastrointestinal tract site, for example, gastrectomy, stomach and intestines suturation, intestinal tract resection and so on (Excluding polypectomy and appendectomy). 6. Individuals with current or history of uterine fibroids, endometriosis, or pelvic organ prolapse. 7. Individuals with a history of uterine or pelvic surgery. 8. Individuals who are receiving hormone replacement therapy (estrogen, progesterone preparations (drinks, patches, ointments), etc.), those who plan to take it during the study period. 9. Individuals who regularly overdose beverages containing diuretic ingredients. 10. Individuals with a history of allergies or asthma. 11. Individuals who regularly take health foods, supplements, and medicines that may affect the test. 12. Be Suspected alcohol or drug dependence. 13. Individuals who have smoked since 3 months of consent. 14. Individuals who participated in other clinical trial at resent (past 84 days). 15. Individuals with irregular lifestyles due to night shifts or shift work. 16. Individuals who live with or will participate in this test. 17. Individuals who cannot comply with the management items during this test. 18. Individuals who work for health food, cosmetics, pharmaceutical companies. 19. Individuals judged inappropriate for the study by the principal.

Study & Design

• Study Type: Interventional
• Study Design: Not specified