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临床试验/EUCTR2007-005679-33-DE
EUCTR2007-005679-33-DE进行中(未招募)1 期

Influence of the selective endothelin receptor-blocker Ambrisetan on the portal pressure in patients with cirrhosis - ADAPT-Studie

Medizinische Fakultät der Martin-Luther-Universität Halle-Wittenberg0 个研究点开始时间: 2010年10月4日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • - Histologically/ laboratory or sonographically confirmed diagnosis of hepatic cirrhosis
  • - Compensated hepatic disease (Child A and B)
  • - Portal hypertension
  • - Age: 18 - 75
  • - Signed, written informed consent
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 24
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 24

排除标准

  • - Acute infection
  • - Hepatic encephalopathy Stadium II- IV
  • - Alcoholic hepatitis and other acute manifestations of hepatitis
  • - Pylethrombosis
  • - Transaminases increased > 3 x UNL
  • - Advanced stadium of cardiac and/or pulmonary preventing head-down position
  • - Evidence of known advanced malignant disease
  • - Usage of beta-blockers within the last 72 hours
  • - Pregnancy or lactation
  • - Participation in another clinical trial
  • - Marked hypotension (systolic blood pressure less than 90 mmHg )
  • - Advanced hepatic disease (stadium Child C)

研究者

发起方
Medizinische Fakultät der Martin-Luther-Universität Halle-Wittenberg

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