Randomized Controlled Trial on Efficacy of Pippalyadi Nabhigat Lepa to Achieve the Progress of Uterine Contractions During 1st Stage of Labour(Sukhaprasav)
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 36
- 试验地点
- 1
- 主要终点
- Improvement and progression of uterine contractions using Partograph before and after the Lepa treatment
研究概览
简要总结
This is open labelled randomized controlled clinical study ,the aim of the study is to evaluate the efficacy of Pippalyadi Nabhigat Lepa to achieve the progress of uterine contractions(Sukhaprasav) during first stage of labour.Total 36 participants will be enrolled in two groups(18 in each group).Group A will be treated with Pippalyadi Nabhigat Lepa and Group B will be observed without Pippalyadi Nabhigat Lepa with required standard of care.The age group for study is 22-35yrs pregnant females with gestational age 36 completed weeks who are in labour.The final conclusion will be drawn on the basis of statistical methods.
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
- 22.00 Year(s) 至 35.00 Year(s)(—)
- 性别
- Female
入选标准
- •All Primigravida and Multigravida with age group between 22yrs to 35yrs with Gestational age 36 completed weeks who are in Labour with Cephalic presentation with Adequate liquor.
排除标准
- •Patient who K/C/O Garbhopdrava like PIH ,Anaemia,Cardiac disease Patients who are K//C/O Garbhavyapad like Intrauterine Growth Retardation,Oligohydramnios,Placenta previa.
结局指标
主要结局
Improvement and progression of uterine contractions using Partograph before and after the Lepa treatment
时间窗: Three times from onset of labour(3-4 hours)-with 1 hour of interval
次要结局
- To observe the adverse effect of Pippalyadi Nabhigat Lepa(Three times from onset of labour(3-4 hours)-with 1 hour of interval)
