ACTRN12612001002875已完成3 期
Efficacy of prothrombin complex in achieving haemostasis compared to standard treatment in adult patients undergoing peritoneal cytoreductive surgery requiring massive transfusion.
适应症
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 80
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomised controlled trial
- 主要目的
- Treatment
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 18 Years 至 o limit（—）
- 性别
- All
入选标准
- •1.Age greater than or equal to 18 years
- •2.Planned for peritonectomy
- •3.Informed consent
排除标准
- •1.Known bleeding disorder
- •2.Known requirement for anti-coagulation e.g. prior DVT/PE requiring anti-coagulation, requirement for caval filter
- •3.Known hypersensitivity to any pooled-blood or recombinant blood products
- •4.Known hypersensitivity to any constituents in Prothrombinex-VF, including know allergy to heparin or a history of heparin-induced thrombocytopenia
- •5. Evidence of active thrombosis or disseminated intravascular coagulation (DIC)
研究者
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