临床试验/CTRI/2024/02/062460

CTRI/2024/02/062460尚未招募Unknown

Study of oral Mifepristone as a cervical ripening agent to induce labour in low-risk full-term live pregnancy beyond 40 weeks of gestation - a randomized controlled trial

Umaid Hospital, Dr SN Medical College1 个研究点分布在 1 个国家目标入组 100 人开始时间: 2024年2月8日最近更新: 2024年1月29日

试验速览

阶段: Unknown
状态: 尚未招募
发起方
入组人数: 100
试验地点: 1
主要终点: Gain in Bishops score

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

Through this study we want to see the effect of indirect labour inducing agent- Mifepristone on cervical ripening in an unripe cervix at term in low-risk pregnant female population. So, in one arm we will give Tab Mifepristone for induction and in the control arm expectant management will be done.

研究设计

研究类型: Observational

入排标准

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

入选标准

•Pregnant females of age between 18-45 years old, Primigravida or Gravida 2, with singleton live pregnancy with cephalic presentation of gestational age 40-41 weeks without any obstetric complications, having an unripe cervix and intact membranes.

排除标准

•Pregnant females having any obstetric complications, any previous uterine surgery, any fetal compromise.

结局指标

主要结局

Gain in Bishops score

时间窗: Baseline, at 24 hours, 48 hours, 72 hours from first dose of Mifepristone

次要结局

1)Duration of induction to active phase of labour & induction to delivery interval.(2)Mode of delivery)

研究者

发起方

Umaid Hospital, Dr SN Medical College

申办方类型

Government medical college

责任方

Principal Investigator

主要研究者

Dr Nikita Yadav

Dr. S.N. Medical College, Jodhpur

研究点 (1)

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