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临床试验/CTRI/2025/05/086934
CTRI/2025/05/086934尚未招募不适用

Randomized Controlled Trial on Efficacy of Pippalyadi Nabhigat Lepa to Achieve the Progress of Uterine Contractions During 1st Stage of Labour(Sukhaprasav)

Pratiksha Limbhore1 个研究点 分布在 1 个国家目标入组 36 人开始时间: 2025年1月6日最近更新:

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)

研究者

发起方
Pratiksha Limbhore
申办方类型
Other [self]

研究点 (1)

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