跳至主要内容
临床试验/PACTR201405000798226
PACTR201405000798226招募中未知

The impact of paracentesis flow rate in patients with liver cirrhosis on the development of paracentesis induced circulatory dysfunction.

ational Liver Institute, Menoufiya University0 个研究点目标入组 60 人开始时间: 2014年3月21日最近更新:
适应症

试验速览

阶段
未知
状态
招募中
发起方
入组人数
60

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 Year(s) 至 70 Year(s)(—)
性别
All

入选标准

  • 1-the presence of tense ascites determined by clinical examination and abdominal ultrasound, requiring frequent therapeutic paracentesis

排除标准

  • 1-arterial hypertension, history of coronary disease, cardiac failure, respiratory disease.
  • 2-hepatic encephalopathy.
  • 4-spontaneous bacterial peritonitis (defined by polymorphonuclear cell count >250/mm3 in ascites
  • 5-elevated creatinine concentration >1.5 mg/dL
  • 6-gastrointestinal bleeding within 7 days before the study.

研究者

发起方
ational Liver Institute, Menoufiya University

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