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临床试验/NCT04199910
NCT04199910暂停不适用

4beta-hydroksikolesteroli Maksakirroosissa

University of Oulu2 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2019年12月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
暂停
入组人数
120
试验地点
2
主要终点
Blood 4beta-hydroxycholesterol concentration

研究概览

简要总结

The aim is to evaluate the levels of oxysterols and especially 4beta-hydroxycholesterol in patients with liver cirrhosis. Three cirrhosis cohorts are recruited: patients treated with spironolactone, patients treated with rifaximin, patients without spironolactone or rifaximin. Also three other control cohorts are recruited: patients with pneumonia, patients with Crohn's disease, patients with ulcerative colitis. The effect of the cirrhosis and its medications spironolactone and rifaximin are compared to control groups.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients with cirrhosis, pneumonia, Crohn's disease or colitis ulcerosa
  • Treated in the ward 42 of the Oulu University Hospital

排除标准

  • 未提供

研究组 & 干预措施

Pneumonia

干预措施: There is no intervention, only research blood samples are collected (Other)

Crohn's disease

干预措施: There is no intervention, only research blood samples are collected (Other)

Ulcerative colitis

干预措施: There is no intervention, only research blood samples are collected (Other)

Liver cirrhosis with spironolactone

干预措施: There is no intervention, only research blood samples are collected (Other)

Liver cirrhosis with rifaximin

干预措施: There is no intervention, only research blood samples are collected (Other)

Liver cirrhosis without spironolactone or rifaximin

干预措施: There is no intervention, only research blood samples are collected (Other)

结局指标

主要结局

Blood 4beta-hydroxycholesterol concentration

时间窗: At the time point of the blood collection - cross-sectional. One day.

Blood 4beta-hydroxycholesterol concentration

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Janne Hukkanen

Professor

University of Oulu

研究点 (2)

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