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
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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