跳至主要内容
临床试验/NCT02258048
NCT02258048撤回不适用

The Use of Transient Elastography to Predict Clinical Decompensation in Patients With Early Cirrhosis

NYU Langone Health1 个研究点 分布在 1 个国家开始时间: 2014年10月最近更新:
适应症

试验速览

阶段
不适用
状态
撤回
试验地点
1
主要终点
Liver Stiffness

研究概览

简要总结

This is a prospective study designed to examine the role of transient elastography as a predictor of clinical decompensation in patients with early cirrhosis. The study objective is to determine if changes in measurements of liver stiffness with transient elastography can identify patients that will have a more rapid progression of cirrhosis and the development of clinical decompensation. The target population is patients with early stage, well-compensated cirrhosis.

Participants of this study will be asked to complete the following procedures: read and sign the informed consent, medical records review (complete medical history, physical examination, laboratory evaluation, endoscopic findings, radiographic findings), undergo transient elastography to measure liver stiffness every three months until the development of clinical decompensation (ascites, variceal bleeding, hepatorenal syndrome, overt hepatic encephalopathy) for up to 2 years.

详细描述

This is a prospective study designed to examine the role of transient elastography as a predictor of clinical decompensation in patients with early cirrhosis. The study objective is to determine if changes in measurements of liver stiffness with transient elastography can identify patients that will have a more rapid progression of cirrhosis and the development of clinical decompensation. The target population is patients with early stage, well-compensated cirrhosis.

This study will attempt to determine if serial measurements of liver stiffness with transient elastography in patients with early cirrhosis can identify patients at risk of morbidity or mortality associated with hepatic decompensation.

For the Screening Visit, the following procedures will be performed:

  1. Patient will read and sign informed consent. Subjects will be given sufficient time to consider, ask questions, and sign the consent forms.
  2. Patient will be assigned a subject number
  3. Patient will be asked to provide demographic information
  4. Patient will be asked to provide a complete medical history and laboratory evaluation
  5. Physical examination including blood pressure, heart rate, height, and weight.
  6. The following assessments will also be performed:
  • Calculation of modified Child Pugh Score: Using the following biochemical variables: Serum Albumin, Total Bilirubin, Serum Creatinine, and INR.
  • MELD Score: Based on a continuous function of Bilirubin, INR, and Creatinine, which uses a continuous variable ranging from 6-40.
  1. 30cc of blood will be obtained, and serum frozen at -80C (freezer located in Dr. Sigal's office) for up to 5 years. The blood will only be accessible to Dr. Sigal and his research team. This blood may be analysed for known markers of liver disease, markers that may be discovered in the future, and/or to identify new markers of liver disease.

研究设计

研究类型
Observational
观察模型
Case Only
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

  • Ambulatory patients with histologic or radiographic evidence of cirrhosis will be screened for participation in the study.
  • Able to provide informed consent
  • MELD score <10
  • No history of ascites, variceal bleeding, hepatorenal syndrome, overt hepatic encephalopathy.

排除标准

  • History of variceal bleeding, ascites, hepatorenal syndrome, or overt hepatic encephalopathy
  • Inability to provide informed consent
  • Body mass index (BMI)>35

结局指标

主要结局

Liver Stiffness

时间窗: 2 years

Liver stiffness will be measured using hepatic elastography.

次要结局

  • Evidence of Portal Hypertension(2 years)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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