CTRI/2024/01/061097尚未招募3 期
Efficacy and safety of carbetocin versus oxytocin in prevention of post partum hemorrhage in high risk women.An Open label randomised controlled trial - nil
DR SMRITI BAG0 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
- 3 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
- •Women of age between 18-35 years of Gestational age of 37-42 weeks
- •Patients who have given written informed consent Women at risk of PPH including
- •Factors resulting in overdistention of the uterus
- •Multiple gestation (eg, twins)
- •Fetal macrosomia
- •Polyhydramnios
- •Nature of labor and delivery
- •Induced labor
- •Precipitous labor (lasting less than 3 hours)
- •Prolonged labor
- •Forceps or vacuum-assisted delivery
- •Cesarean delivery
- •Factors relating to the placenta
- •Abruptio placentae
- •Placenta previa
- •Abnormal implantation
- •High multiparity
- •Preeclampsia
- •Chorioamnionitis
- •Amniotic fluid embolism
- •May precipitate disseminated intravascular coagulation, resulting in consumptive coagulopathy and uncontrolled blood loss
- •Under general Anesthesia
- •Medications
- •Prolonged oxytocin use
- •Magnesium sulfate
- •Anticoagulants
排除标准
- •Gestational age less than 37 or more than 42 weeks
- •History of thromboembolic disorders,
- •Cases suffering from chronic medical diseases (cardiac, hepatic, renal),
- •Not giving consent
研究者
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