JPRN-UMIN000037409已完成未知
Effect of the supplement on edma of the lower limbs in healthy females - A randomized controlled trial - - Effect of the supplement on edma of the lower limbs in healthy females
HUMA R&D CORP0 个研究点目标入组 102 人开始时间: 2019年7月22日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 102
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)Subject with BMI <= 18.5 kg/m2 and >30 kg/m2. 2)Subject who is taking medication or who is currently under medical treatment. 3)Subject who is under exercise therapy or dietetic therapy. 4)Subject who has an allergy for test food (especially milk allergy) . 5)Subject who has or had a history of either medicine or alcohol dependence syndrome. 6)Subject who has or had a history of mental illness (depression) or sleep disturbance. 7)Subject whose lifestyle is extremely irregular. 8)Subject who has an unbalanced diet. 9)Subject who has serious illness or history such as immune disease, brain disease, malignant tumor, diabetes, liver disease (hepatitis), kidney disease or heart disease, thyroid disease, adrenal disease or other metabolic disease. 10)Subject who cannot stop using the health foods, supplements and medicines that may affect edema and fatigue of lower limbs such as Melilotus extract, long pepper extract, BCAA (branched chain amino acid) during the test period. 11)Subject who cannot stop using products to treat the edema of the lower limbs (pressure socks or stockings, and other tings alike) during the study period. 12)Subject who cannot stop taking food and drinks that is specified as health food or food with functional claims, that may affect the edma of the lower limbs during the study period. 13)Subject who cannot stop taking other medications (including Chinese medicine) or supplements during the study period. 14)Subject who has participated in other clinical studies within the last 3 months or is planning to participate in other clinical studies during the study period. 15)Subject who is planning to get pregnant after the day of informed consent or is currently pregnant and lactating. 16)Subject who cannot keep the daily records. 17)Subject who is considered as an inappropriate candidate by the doctor in charge.
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