CTRI/2021/02/030879已完成2 期
To evaluate the efficacy of the test product in improving hair growth rate, hair volume (follicular density), hair fall reduction and hair thinning in healthy subjects - None
Bajaj Consumer Care Ltd0 个研究点目标入组 91 人开始时间: 待定最近更新:
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 91
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
入选标准
- •1.Female subjectsââ?¬• in general good health.
- •2.Subjects in the age group 18-45 years (both the ages inclusive).
- •3.Subjects complaining of hair fall and damage.
- •4.Subjects willing to give a written informed consent and willing to abide by and comply with the study protocol.
- •5.Hair density of >100 and <200 hair follicle per square cm as per Trichoscan measurement.
- •6.Female Subjects falling under Grade 3 - Grade 6 of hair loss severity grade evaluated as per photo numerical 10-point scale (Linear scale for assessment purpose-In Use Scale).
排除标准
- •1.Subjects who have undergone hair growth treatment within 3 months before screening into the study.
- •2.Subjects having any active scalp disease which may interfere in the study ââ?¬â?? dermatologistââ?¬•s judgement.
- •3.Subjects who have taken chemotherapy for cancer in the 6 months prior to start of the study or have a plan to do treatments during study.
- •4.Subjects who have history of alcoholism, smoking, crash dieting and/ or psychiatric disorder including trichotillomania.
- •5.Subjects who have had hair transplant, who have taken pharmaceutical product which cause hirsutism (ex. phenytoin) and finesteride for androgenic alopecia, under medical treatment for hair problems.
- •6.A known history or present condition of allergic response/hypersensitivity to any cosmetic ingredients and pharmaceutical products.
- •7.Subjects on oral medications, undergoing any chemical hair salon treatment-straightening / perming / colour which will compromise the study.
- •8.Subjects who are pregnant or lactating or nursing as established with medical history.
- •9.Menopausal female subjects as determined by medical history.
- •10.Subjects with chronic illness which may influence the cutaneous state.
- •11.Subjects participating in other similar cosmetic or therapeutic trial within last three months.
- •12.Subjects with any history of underlying uncontrolled medical illness including diabetes mellitus, hypertension, HIV, hepatitis, severe anemia, serious disorder of heart and respiratory apparatus or any other serious medical illness.
研究者
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