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临床试验/NCT01307254
NCT01307254Unknown不适用

(BAFLA- Barzilai Fatty Liver and Iron Metabolism Study)

Ornit Cohen1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2011年1月最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
80
试验地点
1
主要终点
grade of fatty liver disease

研究概览

简要总结

The investigators hypothesize that low iron storages protects from and down-grades non-alcoholic fatty liver disease.

The aim of the study is to show the association between the severity of Non-alcoholic fatty liver disease to low iron status.

详细描述

Patients that will pass a CT scan that includes the abdomen will be asked to participate at our study. These patients will be divided into two groups - with and w/o fatty liver. The severity of fatty liver will be determined using the CT scan (as well as other parameters, such as the size of subcutaneous fat layer). Within 72 hours from the scan, a venous blood test will be taken from the enrolled patients (together with a BMI calculation and a blood pressure measurements). In the blood test we will examine liver functions, iron status etc.

This is a preliminary study that will aid in planning future strategies to treat or even prevent fatty liver (one of the epidemics of our century).

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

  • 未提供

排除标准

  • pregnancy
  • unable to sign an informed consent (legally)
  • known solid/hematological malignancy
  • hemoglobinopathy or myelodysplastic disease (not including G6PD deficiency)
  • active or carrier of viral hepatitis
  • treated a drug the cause fatty liver (eg. amiodarone, tetracyclin, HAART, steroid treatment > 3 months)
  • consumption of > 120g ethanol per week
  • primary liver disease (eg. glycogen storage disease)
  • acute intoxication
  • surgery in previous 7 days

结局指标

主要结局

grade of fatty liver disease

时间窗: 1 year

次要结局

未报告次要终点

研究者

发起方
Ornit Cohen
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Ornit Cohen

r&d unit

Barzilai Medical Center

研究点 (1)

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