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QOL evaluation of plant extract for healthy women

QOL evaluation of plant extract for healthy women - QOL evaluation of plant extract for healthy women

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000039084
Enrollment
40
Registered
2020-12-04
Start date
2020-01-14
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy adult

Interventions

intake plant extract food for 8 weeks intake placebo-controlled food for 8 weeks

Sponsors

TTC Co., Ltd
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Females aged from 20 to 69 years old. Subjects who have psychological stress.

Exclusion criteria

Exclusion criteria: 1) Subjects with dysuria, or who are being treated for dysuria. 2) Subjects who have the habit of taking test food. 3) Subjects who have the habit of taking similar healthcare products. 4) Subjects who have a habit of binge drinking. 5) Patients who have serious disease or subjects who have serious disease history. 6) Subjects who take warfarin potassium or antacid. 7) Subjects who has allergies to plants. 8) Subjects who are judged as unsuitable for the study based on the results of clinical and physical examination. 9) Females who are known or suspected to be pregnant, breastfeeding or desire to become pregnant during the trial period. 10) Subjects who are participated in other clinical studies. 11) Subjects who are judged as unsuitable for the study based on the results of lifestyle questionnaire. 12) Subjects who are judged unfit to enroll in this trial by the investigator.

Design outcomes

Primary

MeasureTime frame
Overactive bladder questionnaire (OAB-q), Stress-related VAS, Health-related QOL

Secondary

MeasureTime frame
voiding diary, water intake test

Countries

Japan

Contacts

Public ContactYuki Ito

Kobayashi Pharmaceutical Co., Ltd. Central R&D Laboratory

y.itou@kobayashi.co.jp080-4752-5102

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026