JPRN-UMIN000049200已完成Unknown
Confirmation of improvement effects on skin function by inhalation of citrus oil-inducing odorant - Confirmation of improvement effects on skin function by inhalation of citrus oil-inducing odorant
CPCC Company Limited0 个研究点目标入组 24 人开始时间: 2023年10月13日最近更新:
适应症
试验速览
- 阶段
- Unknown
- 状态
- 已完成
- 发起方
- 入组人数
- 24
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 45years-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 the health-specific/functional/supplementary (e.g., gamma-aminobutyric acid, glucosylceramide, sodium hyaluronate, L-theanine)/health foods, which might affect the test results. (2) Subjects who have taken affecting medicines (e.g., skin roughness-improving drug, and sleeping pill), and have any difficulty in refraining from taking them during this trial. (3) Subjects with the condition of being over-sensitiveness to cold, even during the summer season. (4) Subjects who realized that the subjects themselves must be in a state of menopausal symptom. (5) Subjects with nasal congestion and/or wrong judgement of fragrance. (6) Subjects falling into the habit of smoking within one year before this trial. (7) Subjects having a bruise and/or a hurt near the skin-measuring position (left cheek part). (8) Subjects having their skin roughness due to pollinosis, during this trial. (9) Subjects with excessive suntan, and/or some kind of work/sport outside for a long time. (10) Subjects who are possible to go on a trip, and/or a business one during this trial, which might affect the test-device usage. (11) Subjects who are now under a specific facial care (e.g., facial/body treatment, electric facial, peeling, laser therapy, and hair removal) at an outside agency. (12) Subjects who have previous/current medical history of severe cardiac, hepatic, renal or digestive diseases. (13) Pregnant, lactating women, or possibly pregnant ones. (14) Subjects suffering from atopic/contact dermatitis, and skin hypersensitivity. (15) Subjects who are now under other clinical tests with some kind of medicine and/or health food, or partook in those within four weeks before this trial, or are planning to participate in those after giving informed consent to take part in this trial. (16) Others who have been determined as ineligible for participation, judging from the investigator's opinions.
研究者
相似试验
已完成
Unknown
Verification of improvement effects on skin function by test-food consumptioHealthy female adultsJPRN-UMIN000049702CPCC Company Limited80
已完成
不适用
Verification of skin condition improvement effect by intake of fermented food of lactic acid bacterium N320 straiHealthy adultsJPRN-UMIN000030349Shiba Palace Clinic60
已完成
Unknown
Verification of skin condition improvement effect by intake of foodHealthy female subjectsJPRN-UMIN000046601SOUKE60
尚未招募
Unknown
Verification of skin condition improvement effect by intake of foodHealthy female subjectsJPRN-UMIN000050059SOUKE60
尚未招募
不适用
Evaluation of skin care products for Chinese having consciousness of sensitive skiHealthy adultsJPRN-UMIN000038383Consumer Behaivor Research CORP60