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临床试验/ISRCTN10107246
ISRCTN10107246已完成未知

Safety and efficacy of oral misoprostol for the induction of labor in Papua New Guinean women: low dose regimen versus standard treatment regimen

Papua New Guinea Institute of Medical Research0 个研究点目标入组 262 人开始时间: 2016年8月8日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
262

研究概览

简要总结

2021 Results article in https://pubmed.ncbi.nlm.nih.gov/33734433/ (added 20/04/2021)

研究设计

研究类型
Interventional

入排标准

性别
Female

入选标准

  • 1. Able to complete study informed consent procedures, to understand the benefits of the study and the potential risks and benefits associated with study participation
  • 2. Aged between 18 and 44 years
  • 3. Willing to undergo clinical assessment, including cervical assessments to establish the Bishop score (cervical readiness or softness and dilatation).
  • 4. Willing to come back after four weeks for follow up progress and check up.
  • 5. Third trimester singleton pregnancies in women over 18 years old
  • 6. Bishops score of less than 6
  • 7. Cephalic presentation
  • 8. Hemoglobin concentration of more than 8g/dL

排除标准

  • 1. Multiple pregnancies confirmed with ultrasound examination
  • 2. Previous caesarian sections or other conditions that required surgery on the uterus with uterine scar
  • 3. Chronic illness such as TB, renal failure, other malignancies and heart disease
  • 4. Hemoglobin of less than 8g/dL with symptomatic anemia
  • 5. Unstable or abnormal lie with malpresentation
  • 6. Any high risk cases that require immediate caesarian sections

研究者

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