跳至主要内容
临床试验/JPRN-C000000337
JPRN-C000000337已完成3 期

Randomized controlled trial to evaluate the effects of the surgical instrument LigaSure on reduction of time of liver transection time, compared with the conventional clamp crushing method at the single institution - Randomized controlled trial to evaluate the effects of LigaSure concerning liver transection time

Hepato-Biliary-Pancreatic Surgery Division, Department of Surgery, Tokyo University Hospital0 个研究点目标入组 120 人开始时间: 2006年2月24日最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
120

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
20years-old 至 85years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1.Simultaneous development of other malignant disease (except a colorectal carcinoma associated with liver metastasis) 2.Cases with high-risks of bleeding, for example; platele counts < 50000/mm3, bleeding time > 5min., PT% < 50% 3.Cases in which inflow occulusion is impossible. 4.Cases with bilio-enteric reconstruction 5.Emergency operation case 6.Cases with some complications of heart, lung, and kidney.

研究者

发起方
Hepato-Biliary-Pancreatic Surgery Division, Department of Surgery, Tokyo University Hospital

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