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临床试验/NCT00734227
NCT00734227已完成不适用

TIPS Versus Portacaval Shunt for Acute Bleeding Varices in Cirrhosis

University of California, San Diego1 个研究点 分布在 1 个国家目标入组 153 人开始时间: 1996年7月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
153
试验地点
1
主要终点
Survival

研究概览

简要总结

In unselected cirrhotic patients with acute portal hypertension-related bleeding to compare the effectiveness in control of bleeding, mortality rate, duration of life, quality of life, and economic costs of two widely used treatment measures: (1) emergency transjugular intrahepatic portal-systemic shunt (TIPS), and (2) emergency portacaval shunt.

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
Single (Investigator)

入排标准

性别
All
接受健康志愿者
否

入选标准

  • •All patients with UGI bleeding who are shown to have the findings of cirrhosis and esophagogastric varices or portal hypertensive gastropathy and require 2 or more units of blood transfusion will be included.

排除标准

  • 未提供

研究组 & 干预措施

A

Active Comparator

Randomization: By the blind card method to TIPS or emergency portacaval shunt. Diagnostic Workup: Completed within 6hr. Rapidity of Therapy: Within 24 hr. Failure of Therapy: Bleeding requiring >6u PRBC in first 7 days, or 8 units PRBC during 12 months.

Rescue Crossover Therapy: When primary therapy has failed. Followup: Lifelong data collection on line, analysis by biostatistician Florin Vaida, PhD. External Advisory, Data Monitoring and Safety Committee by 3 senior academicians.

Procedure: Emergency portacaval shunt.

干预措施: Emergency portacaval shunt (Procedure)

B

Active Comparator

Procedure: Emergency TIPS.

干预措施: Emergency TIPS (Other)

结局指标

主要结局

Survival

时间窗: 10 years

次要结局

  • Control of bleeding and quality of life(10 years)

研究者

申办方类型
Other

研究点 (1)

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