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临床试验/JPRN-UMIN000046981
JPRN-UMIN000046981已完成Unknown

Study of the effect of intake of test supplement on urinary voiding in men: A randomized, double blind, and parallel group comparison study - Study of the effect of intake of test supplement on urinary voiding in men

EP Mediate Co., Ltd.0 个研究点目标入组 80 人开始时间: 2023年3月31日最近更新:

试验速览

阶段
Unknown
状态
已完成
入组人数
80

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
30years-old 至 80years-old(—)
性别
Male

入选标准

  • 未提供

排除标准

  • 1) Subjects who are judged to have overactive bladder 2) Subjects diagnosed as having benign prostatic hyperplasia. 3) Subjects with a history of prostate cancer or suspected prostate cancer 4) Subjects who have nocturia more than twice in the bladder diary before start of intake of trial supplement 5) Subjects whose PSA is 4.0 ng/mL or higher 6) Subjects who are undergoing hospitalization/treatment for dysuria, or those who have been judged to require treatments 7) Subjects who are unable to record the urine volume for a designated period 8) Subjects who have urinary tract infection, urinary tract stones, kidney stones, ureteral stones, gallstones, etc. 9) Subjects who are taking health foods, etc. that affect urination at least once a week, or those who wish to take them during the study period 10) Subjects who are currently taking medication or exercise therapy 11) Subjects who have or history diseases such as diabetes, hepatic, renal, or cardiac diseases, or diseases that affect the secretion of adrenal cortical hormones, or other metabolic diseases 12) Subjects who have a disease that requires constant medication, those who have a disease under treatment, those who have a history of serious disease, and those who are scheduled for surgery. 13) Subjects who may develop allergies in relation to the research. 14) Subjects who have participated in other clinical trials within the past month prior to the screening test date. 15) Subjects who have had abnormalities in clinical laboratory values or cardiopulmonary function, and are judged to have a problem participating in the study 16) Subjects whose physical measurements, physical examination values, and clinical examination values were significantly out of the reference range 17) Subjects who are judged to be unsuitable as subjects based on the background survey. 18) Subjects who are judged to be unsuitable as subjects by the principal investigator or the principle investigational doctor.

研究者

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