CTRI/2023/02/049834已完成2/3 期
A Single Arm Clinical Study To Evaluate The Efficacy Of Lodhradi Kwath In GarbhashayaRhas (Involution Of Uterus) In Sutika Awastha (Puerperium)
Dr Geetika1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2023年1月3日最近更新:
试验速览
- 阶段
- 2/3 期
- 状态
- 已完成
- 发起方
- 入组人数
- 40
- 试验地点
- 1
- 主要终点
- Effect of Lodhradi Kwath in GarbhashayaRhas (involution of uterus) which will be assessed metrically by measuring the symphysio fundal height in Sutika Awastha (puerperium)
研究概览
简要总结
THIS IS A SINGLE ARM CLINICAL STUDY .THE AIM OF THE STUDY IS TO EVALUATE THE EFFICACY OF LODHRADI KWATH IN GARBHASHAYARHAS ( INVOLUTION OF UTERUS ) IN SUTIKA AWASTHA (PUERPERIUM). TOTAL 40 PATIENTS WILL BE ENROLLED AND 20 ML LODHRADI KWATH WILL BE GIVEN TWICE A DAY AFTER MEAL .THE AGE GROUP TAKEN FOR THE STUDY IS 21 TO 35 YEARS PUERPERAL WOMEN.
研究设计
- 研究类型
- Interventional
- 分配方式
- Not Applicable
- 盲法
- Open Label
入排标准
- 年龄范围
- 21.00 Year(s) 至 35.00 Year(s)（—）
- 性别
- Female
入选标准
- •mother from 1-42 days after delivery of any mode(normal delivery with or without episiotomy incision, LSCS).
- •primigravida and multiparas with age of 21 to 35 years.
- •written informed consent & voluntarily willing patients.
排除标准
- •patients having history of post partum hemorrhage or any hemolytic disorder or currently suffering from any type of bleeding disease, trauma, or any other malignancy.
- •high risk pregnancies.
- •patient with puerperial complications such as puerperal pyrexia, puerperal sepsis.
结局指标
主要结局
Effect of Lodhradi Kwath in GarbhashayaRhas (involution of uterus) which will be assessed metrically by measuring the symphysio fundal height in Sutika Awastha (puerperium)
时间窗: In normal delivery- 12 days study with follow up on 2nd, 4th and 12th day. | In LSCS- 15 days study with follow up 5th, 7th and 15th day.
次要结局
- To observe the adverse effects of Lodhradi Kwath, if any(In normal delivery- 12 days study with follow up on 2nd, 4th and 12th day.)
研究者
研究点 (1)
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