A randomised standard controlled clinical trial to assess the efficacy of Khadir vati in the management of Shwetpradar

PDEA College Of Ayurveda and Research Centre1 个研究点分布在 1 个国家目标入组 64 人开始时间: 2023年1月24日最近更新: 2023年9月1日

试验速览

阶段: 不适用
状态: 尚未招募
发起方
入组人数: 64
试验地点: 1
主要终点: To compare the efficacy of Khadir Vati and Nagkeshar vati follow up wise result before and after treatment in the management of Shwetpradar with help of Case Record Proforma and Clinical examination

研究概览研究设计入排标准结局指标研究者研究点记录与标识符相似试验

研究概览

简要总结

This study is randomised clinical study parallel group comparing efficacy of Khadir Vati 500 mg 2 tablets twice a day and Nagkeshar Vati 500 mg 2 tablets twice a day in the management of shwetpradar for 14 days in 64 patients.

研究设计

研究类型: Interventional
分配方式: Coin toss, Lottery, toss of dice, shuffling cards etc
盲法: Open Label

入排标准

年龄范围: 18.00 Year(s) 至 45.00 Year(s)（—）
性别: Female

入选标准

•The patients having clinical signs and symptoms of Shwetpradara Yoni Kandu(Itching Vulva) Yoni Daha(Burning) Yoni Srava(Shwetpradar) Lower Abdominal Pain Low Backache.

排除标准

•Pregnant Women Any type of chronic systemic disorders-TB Cancer Patients consuming Oral Contraceptive Pills.

结局指标

主要结局

To compare the efficacy of Khadir Vati and Nagkeshar vati follow up wise result before and after treatment in the management of Shwetpradar with help of Case Record Proforma and Clinical examination

时间窗: 14 days treatment with two follow ups on 7th and 14th day

次要结局

To study the side effect of drugs if any(14 days)

研究者

发起方

PDEA College Of Ayurveda and Research Centre

申办方类型

Private medical college

研究点 (1)

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