TCTR20220930003已完成2 期
Efficacy of Preoperative Intravenous Tranexamic Acid Before Caesarean Section in Placenta Previa : a randomized double blind control trial
none0 个研究点目标入组 60 人开始时间: 2022年9月30日最近更新:
适应症
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 60
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
- 18 Years 至 N/A (No limit)（—）
- 性别
- Female
入选标准
- •1. All pregnant woman with placenta previa diagnosed by transabdominal or transvaginal ultrasound(if not clearly by TAS) confirmed at GA 28 week by obstetricians
- •3.undergoing caesarean delivery for placenta previa include elective c/s at term (37+ week) or emergency c/s due to placenta previa
- •4.Repeat ultrasound confirm before caesarean section
- •5.Age > 18 year and already informed consent
排除标准
- •1. Allergic patient to transamine
- •2. Undergo caesarean section due to placenta previa before GA 28 week
- •3. follow up by ultrasound during antenatal care and diagnosis was changed
- •4. Patient with showed any sign of adherent placenta on ultrasound
- •5. Patient with active cardiac, hepatic, renal disease
- •6. patient with risk factor for VTE such as prior VTE, thrombophilia disease**, hematologic cancer, immobilize patient, first degree relative history of VTE, morbid obesity BMI>40
- •7.Underlying disease of Coagulopathy, thrombocytopenia or on anticoagulant
- •8. patient cannot make decision
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