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临床试验/NCT00730743
NCT00730743已完成不适用

Open Liver Resection With or Without Vascular Inflow Occlusion: a Randomized Control Trial

Chinese University of Hong Kong1 个研究点 分布在 1 个国家目标入组 126 人开始时间: 2008年5月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
126
试验地点
1
主要终点
Operative time

研究概览

简要总结

This study aims to evaluate whether applying inflow vascular occlusion in modern liver resection is associated with better clinical outcome.

Eligible patients are randomly assigned to the two surgical techniques: with or without the application of inflow vascular occlusion.

Patients outcome including liver function recovery, operative time and blood loss are compared.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age > 18 years
  • Child-Pugh Class A or B

排除标准

  • Informed consent not available
  • Presence of portal vein thrombosis, portal vein tumor thrombus, or previous portal vein embolisation
  • Presence of hepatic artery thrombosis, previous transarterial therapy like TACE, or transarterial internal radiation
  • When portal vein resection is anticipated
  • Emergency hepatectomy
  • Ruptured hepatocellular carcinoma
  • Rehepatectomy (repeated liver resection)
  • Adhesion or anatomical variation that preclude safe and successful application of Pringle maneuver
  • When concomitant bowel or bile duct resection is anticipated

结局指标

主要结局

Operative time

时间窗: From skin incision to completion of operation

Operative blood loss

时间窗: From skin incision to completion of operation

次要结局

  • Operative morbidity and mortality(From date of operation to 30-day after operation)
  • Recovery of liver function(From date of operation to date of discharge)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Cheung Yue Sun

Associate Consultant

Chinese University of Hong Kong

研究点 (1)

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