JPRN-UMIN000050147尚未招募Unknown
Confirmation study on skin-improving effects by test-food intakes - Confirmation study on skin-improving effects by test-food intakes
CPCC Company Limited0 个研究点目标入组 44 人开始时间: 2024年2月1日最近更新:
适应症
试验速览
- 阶段
- Unknown
- 状态
- 尚未招募
- 发起方
- 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
- 35years-old 至 50years-old（—）
- 性别
- Female
入选标准
- 未提供
排除标准
- •(1) Subjects who take steadily (not less than three times a week) in affecting health-specific/functional (e.g., sodium hyaluronate, glucosylceramide, astaxanthin)/supplementary/health foods. (2) Subjects who have taken affecting medicines (e.g., moisturizer), and have any difficulty in refraining from taking them, during this study. (3) Subjects having a bruise and/or a hurt near the skin-measuring position (buccal region). (4) Subjects having their skin roughness due to pollinosis. (5) Subjects with excessive suntan, or working and playing sports outside for long hours. (6) Subjects planning to travel abroad during this study. (7) Subjects being under a specific care on their face (e.g., facial treatment, body care, electric facial, peeling, laser therapy, and hair removal) at an outside agency. (8) Subjects with excessive alcohol intake. (9) Subjects having a habit of smoking. (10) Subjects having previous/current medical history of severe cardiac, hepatic, renal or digestive diseases. (11) Subjects with pregnancy, possibly one, or lactating. (12) Subjects with drug and food allergy. (13) Subjects suffering from atopic dermatitis, contact one, and cutaneous sensitivity. (14) Subjects being under other clinical tests with medicine or health food, or partook in those within four weeks to this study, or planning to join those after giving informed consent. (15) Subjects who donated over 200 mL of their blood and/or blood components within a month to this study. (16) Subjects who donated their whole blood (400 mL) within the last four months to this study. (17) Subjects who will be collected in total of their blood (800 mL) within the last twelve months, after adding the blood amounts planning to be sampled in this study. (18) Subjects being determined as ineligible for participation, judging from the principal/sub investigator.
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