CTRI/2022/02/040485已完成未知
An Open Label, Single-Arm, Clinical Study to Evaluate Efficacy and Safety of KeraScalp Hair Serum in subjects with Mild to Moderate Alopecia of Scalp
A Menarini India Private Limited0 个研究点目标入组 30 人开始时间: 待定最近更新:
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 30
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)Age: 18 to 60 years (both inclusive) at the time of consent.
- •2)Sex: Healthy male or non-pregnant/non-lactating female.
- •3)Female subjects of childbearing potential must have a negative urine pregnancy test performed on screening visit and Enrolment.
- •4)Subjects generally in good health.
- •5)Male subjects with Norwood Pattern II to IV of hair loss and female subjects with Ludwig Scale I to II of hair loss.
- •6)Subjects agreeing to undergo blood test for Hb and Thyroid to rule out any abnormalities which may affect treatment.
- •7)Subjects willing to refrain from any other treatment for the main indications for which the study test products are being given during the course of the study.
- •8)Subjects who commit not to use medicated/ prescription shampoos/hair care products (containing Minoxidil / Anti-hair fall agents) or any other hair fall treatment/ hair products other than the test product for the entire duration of the study.
- •9)Subjects who have used other marketed product for hair fall control in the past.
- •10)Subject willing to use test product throughout the study period as instructed.
- •11)Subjects must be able to understand and provide written informed consent to participate in the study.
- •12)Subjects should be willing and able to follow the study protocol to participate in the study.
- •13)Subjects should be willing to allow to take photos of affected areas during the study duration.
排除标准
- •1)Pregnant or breastfeeding or planning to become pregnant during the study period.
- •2)History of any dermatological condition of the scalp other than hair loss and/or dandruff.
- •3)History of prior use of scalp hair growth treatment within 3 months.
- •4)History of any prior hair growth procedures (e.g., hair transplant or laser).
- •5)Subjects who have applied topical treatment for hair loss for at least 4 weeks and any systemic treatment for at least 3 months, prior to their participation in the study.
- •6)History of alcohol or drug addiction.
- •7)Subjects using other marketed hair fall control products during the study period.
- •8)Subjects who have plans of shaving of scalp hair during the course of the study.
- •9)Subjects who are on chronic oral steroids 03 months before initial application and during the study period.
- •10)History or present condition of irritated or visibly inflamed scalp or severe scalp disease.
- •11)Subjects having a history or present condition of an allergic response to any cosmetic products or ingredient of study product.
- •12)Subjects with hair loss due to Autoimmune disorder/ Chemotherapy/ immunosuppressive drugs/ any major illness/ PCOS etc by history
- •13)Subjects participating in other similar cosmetic or therapeutic trial within last two weeks.
- •14)Any other condition which could warrant exclusion from the study, as per the Dermatologistââ?¬•s/investigatorââ?¬•s discretion.
研究者
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