Healthy adult
Conditions
Interventions
Intake of test food once a day for 8 weeks
Sponsors
TTC Co., Ltd
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: 1)Healthy females from 20 to 79 years of age 2)Daytime urinary frequency is more than 8 times
Exclusion criteria
Exclusion criteria: 1) Subjects who have urinary urgency score >= 2, and total score >= 3 in OABSS 2) Subjects who are LUTS/OAB patients or need to treatment of disease 3) Subjects who routinely use dietary supplements and medicines containing the ingredients involved in the test food 4) Subjects who routinely use dietary supplements and medicines that are said to be effective for pollakiuria 5) Subjects who have a urinary calculus or a history of such diseases 6) Subjects who have a disease requiring regular medication or a history of serious diseases for which medication was required 7) Subjects who have a disease requiring treatment or a history of serious diseases 8) Subjects who have possibilities for emerging allergy related to the study 9) Subjects who drink much alcohol 10) Subjects who cannot follow the procedures of various tests to be carried out during this study 11) Subjects who are judged as unsuitable for the study based on the results of clinical and physical examination on preliminary examination 12) Subjects who have participated in other clinical study within the last one month prior to the current study or are planned to participate in other clinical study after informed consent for the current study 13) Subjects who are pregnant or breastfeeding and who are going to become pregnant or breastfeed during the study period 14) Subjects who are judged as unsuitable for the study based on the results of lifestyle questionnaire 15) Subjects who are judged as unsuitable for the study by the investigator
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| OAB-q and Bladder diary before and after 4 weeks and 8 weeks, and OABSS before and after 8 weeks | — |
Countries
Japan
Contacts
Public ContactKotoha Isobe
TTC Co., Ltd. Clinical Research Planning Department
Outcome results
None listed