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临床试验/CTRI/2025/02/080617
CTRI/2025/02/080617尚未招募不适用

Efficacy of Homoeopathic Medicines of Materia Medica Pura in Warts a Single Blind Randomized Controlled Trial

Dr Arpita Priyadarsini1 个研究点 分布在 1 个国家目标入组 68 人开始时间: 2025年2月25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
68
试验地点
1
主要终点
Changes in Dermatological Life Quality Index in cases of warts

研究概览

简要总结

This is a prospective single blind randomized parallel group placebo-controlled trial which aims is to assess and compare the efficacy of homoeopathic medicines of Materia Medica Pura and placebo in the treatment of warts. Warts are the common medical problems. In Homoeopathy, removing the local symptom through external application without addressing the internal disease is considered problematic. Such methods are described as “criminal” since they suppress the symptoms, leaving the underlying disease untreated. Homoeopathy involves the use of powerful internal medicines to eliminate the internal disease, ensuring a complete and lasting cure. Also there has been limited research focusing on the treatment of warts using medicines documented in Materia Medica Pura. therefore, I intend to undertake this trial to research in this particular domain.

The study will be conducted for a period of 18 months. Target sample size will be 68 but considering 20% dropout case total 82 patient need to be enrolled. All patients will be enrolled according to the inclusion and exclusion criteria.  Cases will be diagnosed based on location, shape, and size of the wart’s diameter, size and length of wart will be measured by vernier caliper. A proper homoeopathic case taking proforma will be used to individualize the case.  Patients will be randomized to receive either individualized homoeopathic medicine from Materia Medica Pura (n=41) or placebo (n=41).  Group A- will receive individualized homoeopathic medicines of Materia Medica Pura.  Group B- will be receive similar looking placebo globules. Globules will be administered orally to the patients.  Doses and potency will be selected according to homoeopathic posology as described in Organon of medicine.  Patients will be called for follow-up every 15 days, with the final assessment done in 3 months from the baseline.  Follow-up will be recorded using DLQI. Status of warts will be recorded by using vernier Caliper (Measuring Scale) to show changes in size and dimension of warts.

Expected Outcomes: Reduction in numbers and size of warts, Changes in Dermatological Life Quality Index (DLQI), Reevaluation of Materia Medica Pura in the treatment of warts, and to compare the efficacy of homoeopathic medicines of Materia Medica Pura and placebo in the treatment of warts.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant Blinded

入排标准

年龄范围
18.00 Year(s) 至 70.00 Year(s)(—)
性别
All

入选标准

  • Patients presenting with any type of warts Patients who are able to provide informed consent and comply with the study requirements Patients with no history of homoeopathic medication in the past four months.

排除标准

  • Pregnant and lactating women Patients with a past history of organ transplant surgery Patients with a past history of skin cancer Patients already diagnosed as HIV positive Patients with advanced disease of vital organs Patients under any individualized homoeopathic medication Idiosyncratic patients Hypochondriac patients Patient from foreign country.

结局指标

主要结局

Changes in Dermatological Life Quality Index in cases of warts

时间窗: 3 months to 6 months from base line

次要结局

  • To compare the efficacy of homoeopathic medicines of Materia Medica Pura and Placebo in treatment of warts(3 months to 6 months from base line)

研究者

发起方
Dr Arpita Priyadarsini
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Dr Arpita Priyadarsini

State National Homoeopathic Medical College And Hospital

研究点 (1)

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