CTRI/2025/04/085129尚未招募4 期
TO STUDY THE EFFICACY OF HOMOEOPATHIC MEDICINE ECHINACEA ANGUSTIFOLIA IN THE MANAGEMENT OF CASES OF FURUNCLE: A PROSPECTIVE INTERVENTIONAL SINGLE ARM TRIAL
ANJANA VERMA1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2025年3月6日最近更新:
试验速览
- 阶段
- 4 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 40
- 试验地点
- 1
- 主要终点
- TO EVALUATE THE EFFICACY OF ECHINACEA ANGUSTIFOLIA IN REDUCING THE SYMPTOMS AND DURATION OF FURUNCLES.
研究概览
简要总结
The study is prospective interventional single arm trial to assess the effect of Echinacea Angustifolia in cases of Furuncle. The study will be conducted in 40 participants which will be enrolled in Jawaharlal Nehru Homoeopathic Medical College Hospital, Vadodara, Gujarat, India. Furunculosis Symptoms Score will be used for assessment purpose. The study will be conducted in the time duration of 1 year.
研究设计
- 研究类型
- Interventional
- 分配方式
- Not Applicable
- 盲法
- Not Applicable
入排标准
- 年龄范围
- 18.00 Year(s) 至 40.00 Year(s)（—）
- 性别
- All
入选标准
- •1.All patients of both gender between 18 to 40 years of age.
- •2.All Socio-economic status.
- •3.Presence of one or more boils.
- •4.Patients willing to give informed consent.
排除标准
- •1.Presence of large boils greater than 5cm in diameter or in sensitive area i.e around nose, eyes, lips and genitalia.
- •2.Patient having severe pain, High grade fever greater than 38.5°C or signs of systemic infection i.e. sepsis.
- •3.Presence of immunosuppressive disorders i.e. HIV/AIDS, Cancer.
- •4.Pregnant or breastfeeding women.
结局指标
主要结局
TO EVALUATE THE EFFICACY OF ECHINACEA ANGUSTIFOLIA IN REDUCING THE SYMPTOMS AND DURATION OF FURUNCLES.
时间窗: 2 MONTHS
次要结局
- TO STUDY THE EFFICACY OF ECHINACEA ANGUSTIFOLIA IN MANAGEMENT OF CASES OF FURUNCLE BY USING(FURUNCULOSIS SYMPTOMS SCORE(FSS).)
研究者
研究点 (1)
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