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临床试验/CTRI/2023/10/058541
CTRI/2023/10/058541尚未招募2/3 期

A Randomized, Parallel Group, Open Label, Active Controlled Clinical Study to Evaluate the Efficacy and Safety of a Unani Pharmacopeial Formulation Marham Hina in the Management of Buthur Labaniyya (Acne Vulgaris).

National Research Institute of Unani Medicine for Skin Disorders1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2023年10月16日最近更新:

试验速览

阶段
2/3 期
状态
尚未招募
发起方
入组人数
60
试验地点
1
主要终点
25% Reduction in Global Acne Grading System Score from baseline

研究概览

简要总结

Buthur Labaniyya(Acne Vulgaris) is the most common skin disease, affect 9.4% of the global population, making it the eighth most prevalent disease worldwide. According to the GBD study, acne vulgaris affects ~85% of young adults’ aged 12–25 years. Acne causes disfigurement which leads to great psychological, emotional and social impact. Anxiety, depression, bullying, lack of confidence, social withdrawal, feelings of insecurity and inferiority even suicidal ideation. In conventional therapy, there are many drugs are available but none of them are free from side effects. Marham hina, is a potent topical treatment from National Formulary of Unani Medicine for Acne Vulgaris.

This Randomized, Active controlled, Parallel Group, Open Label, Clinical study has planned to evaluate the Efficacy and Safety of Marham Hina in the management of acne vulgaris. Participants fulfilling inclusion and exclusion criteria will be receive either test or control drug as per randomization, in test group participants will be receive Marham Hina ointment local application twice  daily at affected sites as per requirement, in control drug participants will be given benzoyl peroxide 2.5% gel topically twice daily at affected sites as per requirement.  Laboratory investigation will be done at baseline and last follow up. Duration of the study is 6 weeks. For  statistical analysis Student t test will be used to find the statistically significant difference in the parameters within the group/ inter the group.  All the result analysis will be done using MS excel 2019.

研究设计

研究类型
Interventional
分配方式
Permuted block randomization, fixed
盲法
Open Label

入排标准

年龄范围
12.00 Year(s) 至 30.00 Year(s)(—)
性别
All

入选标准

  • Participants of any gender in the age group between 12 to 30 years.
  • Participants having any of the following symptoms of Buthur Labaniyya as Comedones, Papules,Pustules ,Nodules, Itching , Erythema.
  • Participants who are willing to participate and comply with the protocol and to sign IEC approved informed consent / assent form.

排除标准

  • Participants aged <12 years and > 30 years.
  • Participants with other variants of acne like acne fulminans, acne rosacea, acne necrotica.
  • Participants suffering from other concomitant diseases like vitiligo, dermatophytosis, psoriasis and eczema.
  • Pregnant or Nursing Women.

结局指标

主要结局

25% Reduction in Global Acne Grading System Score from baseline

时间窗: 6 Weeks

次要结局

  • 1.Reduction in Cooks Acne Grading Scale , Dermatology Life Quality Index , Visual Analogue Scale Score from baseline(2. Improvement in symptoms from baseline)

研究者

发起方
National Research Institute of Unani Medicine for Skin Disorders
申办方类型
Research institution and hospital

研究点 (1)

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