CTRI/2022/12/048597尚未招募Phase 3 4
Evaluate the efficacy of Kareeradi Kwath versus Panchvalkal Kwath (as Yoni Prakshalan) in the management of Shwetapradar (leucorrhoea): A randomized controlled trial
Dr Pooja Basanl1 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1日最近更新:
试验速览
- 阶段
- Phase 3 4
- 状态
- 尚未招募
- 发起方
- 入组人数
- 60
- 试验地点
- 1
- 主要终点
- evaluate the efficacy of Kareeradi Kwatha (as Yoni Prakshalan) in Shweta Pradara (leucorrhoea)
研究概览
简要总结
The volunteers will be informed about the study protocol. willing participants will be randomlyselected as per computer generated table. Clinical research format will be prepared and validated.Prior to the study approval will be taken from IEC, MGACH RC, Salod (H) Wardha and CTRIregistration will be done. After selection, each participant will be tested individually and selectedaccording to selection criteria. They will be divided into two groups as the trial is a parallel group,randomized, open clinical, standard controlled trial. It will include a 16 days treatment period andfollow up.
研究设计
- 研究类型
- Interventional
- 分配方式
- Computer generated randomization
- 盲法
- Participant Blinded
入排标准
- 年龄范围
- 18.00 Year(s) 至 55.00 Year(s)（—）
- 性别
- All
入选标准
- •Female patients from Age 18 year to 55 year in reproductive period of life will be included in this study irrespective of marital status Married/unmarried female’s patients will be taken for this study Female patients having signs and symptoms of Shweta Pradaraa will be included.
排除标准
- •Female patients having signs and symptoms of abnormal Vaginal Bleeding such as menorrhagia metrorrhagia Female patients having pregnancy will be excluded from this study Female patients having Hormonal misbalance diabetes HTN Those patients who are having carcinoma or other severe systemic illness.
结局指标
主要结局
evaluate the efficacy of Kareeradi Kwatha (as Yoni Prakshalan) in Shweta Pradara (leucorrhoea)
时间窗: 16 days
次要结局
- evaluate the efficacy of Panchvalkal Kwath (as Yoni Prakshalan) in Shweta Pradara (leucorrhoea)
研究者
研究点 (1)
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