CTRI/2023/02/050000尚未招募不适用
Usefulness of individualized homoeopathic medicine in centesimal potency vis a vis LM potency in the treatment of tinea corporis: A comparative observational study
Bakson Homoeopathic Medical college and hospital2 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2023年1月3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
- 60
- 试验地点
- 2
- 主要终点
- Expected reduction in 5 D Pruritus scale
研究概览
简要总结
This study is randomized, open label, double arm trial, comparing the usefulness of individualized homoeopathic centesimal potency and LM potency in the management of Tinea corporis. The primary outcome will be to compare the changes in the lesions of Tinea corporis with individualized homoeopathic medicines in centesimal potency and LM potency using 5D Pruritus scale. 5D Pruritus Scale will be used at the baseline, and at the end of treatment or final follow up and the scores in both the groups will be compared and concluded accordingly.
研究设计
- 研究类型
- Interventional
- 分配方式
- Other
- 盲法
- Open Label
入排标准
- 年龄范围
- 19.00 Year(s) 至 59.00 Year(s)(—)
- 性别
- All
入选标准
- •1 Patient with the age group of 19 years to 59 years 2 Diagnostic criteria will be mainly based on clinical history, presentation and examination with the help of KOH test.
- •3 Patient taking prior medications or topical creams will be enrolled after wash out periods of 15 days.
排除标准
- •1 Pregnant and lactating women.
- •2 Patient having tinea infection secondary to other complications like lichenification.
- •3 Immune suppressed patients with HIV or on chemotherapy.
结局指标
主要结局
Expected reduction in 5 D Pruritus scale
时间窗: 5 D Pruritus score will be done at baseline, 4 weeks, 8 weeks and 12 weeks.
次要结局
未报告次要终点
研究者
研究点 (2)
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