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临床试验/CTRI/2025/10/095533
CTRI/2025/10/095533尚未招募不适用

Randomized control trial to find the effectiveness of Individualized Homoeopathic medicine in the treatment of Acne Vulgaris.

Neha Sharma1 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2025年11月12日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
90
试验地点
1
主要终点
Homoeopathic medicines are effective in treatment of Acne Vulgaris in both males and females by using symptom assessment scale Comprehensive Acne severity Scale

研究概览

简要总结

Acne Vulgaris is a widespread skin condition making it a vital topic for research and study. It is one of the most prevalent dermatological conditions, particularly among adolescents and young adults. The reason for choosing this topic is to evaluate the effectiveness of individualized homoeopathic medicines using a randomized control trial design and to provide evidence based validation for homoeopathic intervention in Acne Vulgaris. Randomized control trial minimize bias ensure high internal validity and establish cause and effect relationship. This study aims to build upon existing research providing further evidence on effectiveness  of individualized homoeopathic medicine in treating Acne Vulgaris .Therefore in in this i am to explore individualized  remedies thar addresses both the physical symptoms and underlying emotional factors aligning with the core principles of homoeopathic medicines.

研究设计

研究类型
Interventional
分配方式
Coin toss, Lottery, toss of dice, shuffling cards etc
盲法
Participant Blinded

入排标准

年龄范围
15.00 Year(s) 至 35.00 Year(s)(—)
性别
All

入选标准

  • Mild to severe Acne Patient is willing to participate in the study and provide informed consent.

排除标准

  • Underlying conditions presence of PCOS hormonal imbalance or other condition affecting acne Facial skin conditions that could confound assessments such as dermatitis psoriasis concurrent medications pregnancy and lactation during the study.

结局指标

主要结局

Homoeopathic medicines are effective in treatment of Acne Vulgaris in both males and females by using symptom assessment scale Comprehensive Acne severity Scale

时间窗: Before exams of part 2

次要结局

未报告次要终点

研究者

发起方
Neha Sharma
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Neha Sharma

SGNHMCRI Tantia University

研究点 (1)

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