JPRN-UMIN000049157已完成Unknown
Effects of consumption of the test food on unidentified complaints of menstruation in healthy Japanese women: a randomized, placebo-controlled, double-blind, parallel-group comparison study - Effects of consumption of the test food on unidentified complaints of menstruation in healthy Japanese women
适应症
试验速览
- 阶段
- Unknown
- 状态
- 已完成
- 入组人数
- 44
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
- 20years-old 至 40years-old（—）
- 性别
- Female
入选标准
- 未提供
排除标准
- •1. Subjects who are undergoing medical treatment or have a medical history of malignant tumor, heart failure, and myocardial infarction 2. Subjects who have a pacemaker or an implantable cardioverter defibrillator (ICD) 3. Subjects currently undergoing treatment for any of the following chronic diseases: cardiac arrhythmia, liver disorder, kidney disorder, cerebrovascular disorder, rheumatism, diabetes mellitus, dyslipidemia, hypertension, or any other chronic diseases 4. Subjects who are undergoing medical treatment or have a medical history of gynopathy {such as premenstrual syndrome (PMS), premenstrual dysphoric Disorder (PMDD), secondary amenorrhea, dysmenorrhea, endometriosis, hysteromyoma, breast cancer, cervical cancer, endometrial carcinoma, and ovarian cancer} 5. Subjects without menstrual pain or symptoms associated with menstruation at all 6. Subjects who have severe menstrual pain that cannot be controlled with analgesics 7. Subjects who are undergoing medical treatment or have a medical history of psychiatric disorder 8. Subjects who receive hormonal therapy 9. Subjects who are currently taking low dose pill 10. Postmenopausal subjects 11. Subjects who use or take "Foods for Specified Health Uses," or "Foods with Functional Claims" in daily 12. Subjects who are currently taking medications (including herbal medicines) and supplements 13. Subjects who are allergic to medicines and/or the test food related products 14. Subjects who are pregnant, lactating, or planning to become pregnant during this trial 15. Subjects who suffer from COVID-19 16. Subjects who have been enrolled in other clinical trials within the last 28 days before the agreement to participate in this trial or plan to participate another trial during this trial 17. Subjects who are judged as ineligible to participate in this study by the physician
研究者
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