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临床试验/CTRI/2018/03/012303
CTRI/2018/03/012303进行中(未招募)1 期

Clinical evaluation of the safety and efficacy of the investigational product containing herbal actives for hair growth and hair quality in subjects experiencing hair loss - NI

Dabur Research Foundation0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
1 期
状态
进行中(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 subjectsâ?? in general good health.
  • 2.Subjects in the age group 18-45 years (both the ages inclusive).
  • 3.Subjects willing to give a written informed consent and agree to come for a regular follow up visit.
  • 4.Subjects with hair fall- above 20 hair fall in comb test (with bulb+ without bulb)
  • 5.Subjects with follicular density above 100-200
  • 6.Subjects complaining of hair fall
  • 7.Subjects complaining about hair thinning
  • 8.Subjects who have not participated in a similar investigation in the past three months.
  • 9.Healthy volunteers with no known allergy as established by medical history.
  • 10.Subjects who do not smoke or drink
  • 11.Subjects who are not crash dieting.
  • 12.Subjects who agree to refrain from using hair dye / hair color during the study period.
  • 13.Subjects willing to refrain from any type of hair treatment like perming, straightening etc. during the study duration.
  • 14.Subjects with regular oiling habits

排除标准

  • 1.A known history or present condition of allergic response/hypersensitivity to any cosmetic ingredients and pharmaceutical products.
  • 2.Subjects who have had hair transplant.
  • 3.Subjects who take pharmaceutical product which cause hirsutism (ex. phenytoin) and finesteride for androgenic alopecia
  • 4.Subjects who have undergone hair growth treatment within 3 months before screening into the study.
  • 5.Subjects having any active scalp diseasewhichmayinterfere in the studydermatologistâ??sjudgement.
  • 6.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.
  • 7.Subjects who have history of alcoholism and/ or psychiatric disorder including trichotillomania.
  • 8.Subjects consuming alcohol and smoking
  • 9.Subjects on oral medications which will compromise the study.
  • 10.Subjects who are pregnant or lactating or nursing as established with medical history.
  • 11.Under medical treatment for hair problems
  • 12.Undergoing any chemical hair salon treatment-
  • straightening / perming / colour
  • 13.Menopausal female subjects as determined by medical history.
  • 14.Pregnant female subjects as determined by UPT test
  • 15.Chronic illness which may influence the cutaneous state. Subjects participating in other similar cosmetic or therapeutic trial within last three months
  • 16.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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