EUCTR2014-004809-33-ES进行中（未招募）1 期
Albumin infusion effects in patients with cirrhosis hepatic encephalopathy
Fundació Hospital Universitari Vall d'Hebron - Institut de Recerca (VHIR)0 个研究点目标入组 140 人开始时间: 2015年1月12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
- 入组人数
- 140
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
- •1. Age between 18 and 85 years.
- •2. Liver cirrhosis defined by previous clinical data or liver biopsy.
- •3. Presence of an episode of acute hepatic encephalopathy of grade> 2.
- •4. Sign the 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 140
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 140
排除标准
- •1. Pregnant or breast-feeding.
- •2. Terminal illness.
- •3. Presence of Acute-on-chronic liver failure.
- •4. Needing for intensive support measures.
- •5. Active gastrointestinal bleeding.
- •6. neurological or psychiatric comorbidity that hinders the assessment of hepatic encephalopathy.
- •7. Clinical situations in which it is contraindicated to administer intravenous albumin.
- •8. MELD score less than 15 or greater than 25 at the time of inclusion
- •9. Any medical condition previous to patient inclusion in the study involving administration of albumin during a previous 7 day period.
研究者
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