CTRI/2019/11/021901进行中（未招募）未知
Minimum Effective Dose of Oxytocin Bolus during Cesarean Section Delivery: Comparison between Patients at High versus Low Risk of Uterine Atony - NI
niversity College of Mediacl Sciences and GTb Hospital0 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
- 未知
- 状态
- 进行中（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
- •>18 years, and posted for cesarean section will be evaluated for inclusion.
- •Those with ââ?°Â¥ 1 risk factor for uterine atony will be included into group H (i.e., high risk group), and with lack of any such factor into group L (i.e., low risk group). The various high-risk factors for uterine atony will include multiple gestation, polyhydramnios, macrosomia, uterine fibroid, previous uterine surgery, abnormal placentation, history of previous uterine atony or PPH, high parity (ââ?°Â¥ 5 previous delivery), chorioamnionitis (fever and on antibiotics for same), magnesium sulfate therapy, or need for general anesthesia.
排除标准
- •Exclusion criteria will include patient refusal, active labor ( >3 cm cervical dilation), use of prior oxytocin for labor induction and/or augmentation, pre-eclampsia without magnesium sulfate therapy and absence of any pre-defined high-risk for uterine atony, coagulopathy (thrombocytopenia with platelet count <50,000/mm3 or INR >1.5), as well as history of bleeding disorder or heart disease.
研究者
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