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临床试验/NCT02505113
NCT02505113Unknown不适用

Cavernous Transformation of Portal Vein: Etiology, Diagnosis, Management and Prognosis

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月最近更新:
适应症
干预措施
相关药物

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
Ascites Volume (mL)

研究概览

简要总结

To observe the etiology, diagnosis, management and prognosis of cavernous transformation of portal vein.

详细描述

To observe the etiology, diagnosis, management and prognosis of cavernous transformation of portal vein.

We perform Montelukast (10mg, q.d., p.o.) fot the treatment of symptomatic cavernous transformation of portal vein and to observe the efficacy such as the decrease of the volume of ascites and hydrothorax.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Prospective

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 CTPV.

排除标准

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

研究组 & 干预措施

CTPV treated with Montelukast

Patients with CTPV treated with Montelukast (10mg, q.d., p.o.).

干预措施: Montelukast (Drug)

结局指标

主要结局

Ascites Volume (mL)

时间窗: 6 month

Ascites measured by CT scanning or ultrasound (If the patients had the history of ascites before)

Hydrothorax Volume (mL)

时间窗: 6 month

Hydrothorax measured by CT scanning or ultrasound (If the patients had the history of hydrothorax 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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