PACTR202310744034060尚未招募3 期
Safety And Efficacy Of Sublingual Versus Vaginal Misoprostol For Labour Induction Among Primigravida At Term: A Randomised Controlled Trial
Dr. Aituma Lewis Osadebamwen0 个研究点目标入组 82 人开始时间: 2023年9月30日最近更新:
试验速览
- 阶段
- 3 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 82
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
- 年龄范围
- 19 Year(s) 至 44 Year(s)（—）
- 性别
- Female
入选标准
- •Gestational age =37 to 42 weeks.
- •Participants who have indication for induction of Labour.
- •Cervical assessment with Modified Bishops score value of less than 6.
- •Singleton gestation.
- •Cephalic presentation.
- •Optimal biophysical profile.
- •Participants who gave written consent to participate in the study.
排除标准
- •Teenage pregnancy.
- •Participants who withdraw consent even after being enrolled into the sudy.
- •All indications for Cesarean section.
- •Participants with relative or absolute contraindications to misoprostol use (e.g.; misoprostol allergies, Acute Cerebrovascular Disease, Coronary Artery Disease, epileptics).
- •A history of extensive uterine surgery.
- •Abnormal vaginal bleeding.
- •An unconscious patient.
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