A study of efficacy of plant-derived product in female with voiding dysfunction.
- Conditions
- Healthy adult
- Registration Number
- JPRN-UMIN000022829
- Lead Sponsor
- TTC Co.,Ltd
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- Female
- Target Recruitment
- 15
Not provided
1) LUTS/OAB patients or subjects who need to treatment of disease. 2) Subjects who have the habit of taking test food. 3) Subjects who have the habit of taking 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) Urinary calculus or bladder calculus. 9) Subjects who are judged as unsuitable for the study based on the results of clinical and physical examination. 10) Females who are known or suspected to be pregnant, breastfeeding or desire to become pregnant during the trial period. 11) Subjects who are participated in other clinical studies. 12) Subjects who are judged as unsuitable for the study based on the results of lifestyle questionnaire. 13) Subjects who are judged unfit to enroll in this trial by the investigator.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method