| Unique ID issued by UMIN | UMIN000059739 |
|---|---|
| Receipt number | R000068313 |
| Scientific Title | Study on the Effects of Test Food Intake on Urinary Discomfort in Women: Open-label study |
| Date of disclosure of the study information | 2026/07/16 |
| Last modified on | 2026/07/15 13:55:20 |
Study on the Effects of Test Food Intake on Urinary Discomfort in Women
Test Food Intake for Urinary Discomfort
Study on the Effects of Test Food Intake on Urinary Discomfort in Women: Open-label study
Test Food Intake for Urinary Discomfort: Open-label study
| Japan |
To examine the effects of test food intake on urinary discomfort in women
| Not applicable | Adult |
Others
NO
To examine the effects of test food intake on urinary discomfort in women
Efficacy
urine test
Core Lower Urinary Tract Symptom Score
Interventional
Parallel
Randomized
Cluster
Double blind -all involved are blinded
Placebo
2
Prevention
| Food |
Participants will consume the test food for 4 weeks.
They will take one packet per day with water or lukewarm water.
Participants will consume the placebo for 4 weeks.
They will take one packet per day with water or lukewarm water.
| 18 | years-old | <= |
| 75 | years-old | >= |
Female
(1) Individuals who are generally considered to be healthy
(2) Women who subjectively experience mild urinary discomfort (e.g., pain during urination, cloudy urine, or residual urine sensation) several times a year
(3) Individuals who can give voluntary written consent to participate in the present trial
(1) Individuals who regularly consume any dietary supplements, quasi-drugs, or medicines that have the same or similar effects as those evaluated in this study
(2) Individuals who have changed or newly started taking health foods or dietary supplements within the past 4 weeks
(3) Individuals who work night shifts or rotating shifts
(4) Individuals receiving medical or preventive treatment (e.g., hormone replacement, pharmacotherapy, exercise, or dietary therapy) at the time of obtaining informed consent, or judged to require such treatment
(5) Individuals with a history of serious metabolic, hepatic, renal, cardiovascular, respiratory, endocrine, immune, neurological, or psychiatric disorders.
(6) Individuals with a medical history of alcohol or drug dependence
(7) Individuals who might develop an allergic reaction to foods
(8) Individuals who are pregnant, breastfeeding, or intend to become pregnant during the study period
(9) Individuals who have participated in any other human study involving foods, medicines, quasi-drugs, or medical devices within the past 4 weeks, or who plan to participate in another study during the study period
(10) Individuals who are judged by the investigator to be unsuitable for participation in the study
30
| 1st name | Koichiro |
| Middle name | |
| Last name | Ohnuki |
User Life Science Co.,Ltd.
The research and development part
8200115
372-3,Niho,Iiduka-shi,Fukuoka,Japan
0948823123
ohnuki.rinp@gmail.com
| 1st name | Keiko |
| Middle name | |
| Last name | Ohnuki |
User Life Science Co.,Ltd.
The research and development part
8200115
372-3,Niho,Iiduka-shi,Fukuoka,Japan
0948823123
userlifescience@gmail.com
Others
Others
Profit organization
User Life Science Co., Ltd. Ethics Committee
372-3,Niho,Iiduka-shi,Fukuoka,Japan
0948823123
keiwithmogu@gmail.com
NO
福岡県
| 2026 | Year | 07 | Month | 16 | Day |
Unpublished
Completed
| 2025 | Year | 10 | Month | 31 | Day |
| 2025 | Year | 03 | Month | 11 | Day |
| 2025 | Year | 11 | Month | 12 | Day |
| 2025 | Year | 12 | Month | 31 | Day |
| 2025 | Year | 11 | Month | 11 | Day |
| 2026 | Year | 07 | Month | 15 | Day |
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000068313