PACTR202607696756780进行中（未招募）不适用
A prospective randomized controlled trial comparing temporary tourniquet application versus bilateral uterine artery ligation for reducing intraoperative blood loss during surgical management of placenta previa major with suspected placenta accreta spectrum
适应症
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 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 Year(s) 至 44 Year(s)（—）
- 性别
- Female
入选标准
- •Pregnant women aged 18 years or older.
- •Gestational age =34 weeks.
- •Singleton pregnancy.
- •Placenta previa major diagnosed by ultrasonography.
- •Suspected placenta accreta spectrum based on ultrasound with or without MRI.
- •Planned elective cesarean delivery.
- •Ability and willingness to provide written informed consent
排除标准
- •Emergency cesarean section due to uncontrolled hemorrhage.
- •Confirmed placenta percreta with planned cesarean hysterectomy.
- •Known coagulation or bleeding disorders.
- •Multiple pregnancy.
- •Major fetal congenital anomalies or intrauterine fetal demise.
- •Severe maternal medical illness contraindicating study participation.
- •Refusal to participate in the study.
研究者
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