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临床试验/CTRI/2022/02/040485
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

发起方
A Menarini India Private Limited

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