跳至主要内容
临床试验/NCT02504034
NCT02504034Unknown不适用

Interventional Radiology for the Treatment of Symptomatic Portal Hypertension in Patients With Cavernous Transformation of Portal Vein

Sun Yat-sen University1 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2010年10月1日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
150
试验地点
1
主要终点
Incidence Rate of Gastrointestinal Bleeding

研究概览

简要总结

To evaluate the values of portosystemic shunt and other interventional radiology approaches for treatment of symptomatic portal hypertension in patients with cavernous transformation of portal vein.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
1 Year 至 80 Years(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • All patients with portal hypertention who have enough image information to confirm cavernous transformation of portal vein.

排除标准

  • Patients with known severe dysfunction of heart, lung, brain, kidney and other vital organs.

结局指标

主要结局

Incidence Rate of Gastrointestinal Bleeding

时间窗: 1 month

No gastrointestinal bleeding proved by patients' symptoms (If the patients had the history of gastrointestinal bleeding before)

Ascites Volume (mL)

时间窗: 1 month

No ascites proved by CT scanning or ultrasound (If the patients had the history of ascites before)

次要结局

未报告次要终点

研究者

发起方
Sun Yat-sen University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Zaibo Jiang

Department of Radiology, The Third Affiliated Hospital, Sun Yat-Sen University

Sun Yat-sen University

研究点 (1)

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