CTRI/2023/11/059372尚未招募4 期
Sequential versus simultaneous use of High- volume Foley’s Catheter and Misoprostol for Induction of Labour: A Randomised Control Trial - NI
Free Maternity Services Government of India under National Health Mission0 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
- 4 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
- •All nulliparous women with unfavorable cervix (Bishop score <6) planned for IOL. Inclusion criteria will be ; age 18 to 40 years and singleton-term pregnancy (=38 weeks).
排除标准
- •spontaneous labor; Bishop score =6; fetal malpresentation; non-reassuring fetal heart rate; any previous uterine surgery (CD/hysterotomy, myomectomy, or metroplasty); multifetal gestation; antepartum hemorrhage; intrauterine fetal demise; rupture of membranes; placenta previa or vasa previa, or cord presentation; active genital herpes; severe pre-eclampsia, GDM on pharmacological treatment
- •any contraindication to vaginal delivery; allergy to latex; any contraindication to prostaglandins; any medical illness such as asthma, cardiac disease, known bleeding disorder, concurrent anticoagulant therapy, pelvic infection, any comorbid surgical illness (eg, nephrolithiasis, cholelithiasis); or any previous attempt of IOL in the present pregnancy)
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