CTRI/2022/09/045885尚未招募2 期
SAFETY AND EFFICACY OF ORAL MIFEPRISTONE VERSUS INTRACERVICAL DINOPROSTONE GEL AS A CERVICAL RIPENING AGENT AMONG PREGNANT WOMEN REQUIRING LABOUR INDUCTION ââ?¬â?? A RANDOMIZED CONTROL TRIA
Dr P Srirohini0 个研究点目标入组 0 人开始时间: 待定最近更新:
试验速览
- 阶段
- 2 期
- 状态
- 尚未招募
- 发起方
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •1. Willing to participate
- •2. Primigravida
- •3. Singleton pregnancy,Cephalic presentation.
- •4. Gestational age 40+ weeks.
- •5. Maternal age >19years
- •6. No contraindications for prostaglandins or mifepristone.
- •7. No contraindication for vaginal delivery
- •8. Modified Bishopââ?¬•s Score < 6
- •9. Intact membranes.
- •10.Women with history of 1 or 2 previous abortions.
排除标准
- •Breech presentation
- •Cephalopelvic disproportion
- •History of 3 or more abortions
- •Estimated fetal weight > 4.5 kg or < 2kg
- •Multigravida,Twin pregnancy
- •Obstetric complications like Diabetes ,Abruptio placenta or Placenta previa.
- •Abnormal fetal heart rate patterns.
- •Premature rupture of membranes.
- •Active genital infection.
- •Contraindication for mifepristone
- •Chorioamnionitis
- •Myoma or uterine anomalies
- •IVF Conception
研究者
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