CTRI/2024/03/063657尚未招募2 期
To evaluate the safety and efficacy of the test products in comparison to baseline in improving hair growth rate and reducing hair fall among healthy subjects - NI
试验速览
- 阶段
- 2 期
- 状态
- 尚未招募
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.Male and female subjects in general good health.
- •2.Subjects in the age group 18-50 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 greater than 100 and less than 200 hair follicle per square cm as per TrichoScan measurement
- •6.Male and female Subjects falling under Grade 3 - Grade 6 of hair loss severity grade evaluated as per MSCR photo numerical 10-point scale (Linear scale for assessment purpose-In Use Scale).
排除标准
- •1 Subjects who have undergone any kind of hair growth treatment in the last 3 months
- •2 Subjects having any active but controllable scalp disease which may interfere in the study assessments
- •3 Subjects who have taken chemotherapy for cancer in the 6 months prior to the studys start
- •4 Subjects who have history of crash dieting and or psychiatric disorder including trichotillomania
- •5 Subjects who have undergone hair transplant
- •6 A known history or present condition of allergic response or hypersensitivity to any topical or oral cosmetic pharmaceutical or nutraceutical product
- •7 Subjects on oral medications like topical or systemic corticosteroids undergoing any chemical hair salon treatment which will compromise the study
- •8 Subjects with chronic illness which may influence the cutaneous state
- •9 Subjects who are pregnant or nursing Self declared
- •10 Subjects with any history or present of underlying uncontrolled medical illness or any other serious medical illness
研究者
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