跳至主要内容
临床试验/NCT01758939
NCT01758939Unknown不适用

Phase 4 Predictors of Response to Combined Pegylated Interferon and Ribavirin in Chronic Hepatitis C Genotype IV Infected Egyptian Patients

Cairo University1 个研究点 分布在 1 个国家目标入组 100,000 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
入组人数
100,000
试验地点
1
主要终点
Assess the response to the Interferon therapy.

研究概览

简要总结

Retrospective prospective cohort study aimed at Assessing the predictors to the response to the antiviral combined therapy with pegylated Interferon (Both types: Alfa 2 A and Alfa 2 B) in hepatitis C virus infected Egyptian patients.

详细描述

Retrospective prospective cohort study conducted on HCV infected patients treated with Interferon alpha therapy, the retrospective part of the study includes the data of the patients retrieved from medical records from the period from September 2006 till January 2011. Then from January 2011 the study became prospective national study. Responders to therapy were defined by normalization of serum alanine aminotransferase (ALT) and absence of detectable serum HCV RNA at the end of treatment (48 weeks). Relapsed responders to therapy were defined by normalization of serum ALT and absence of detectable serum HCV RNA at the end of treatment but with an increase of the serum ALT and the presence of HCV RNA at follow-up 72 weeks). Non-responders were defined by elevated serum ALT and the presence of HCV RNA at the end of treatment. All patients will sign a written informed consent to share in this clinical registry by their data and biological samples. Sub-studies will be conducted on subgroups of patients sharing in this main study after signing a written informed consent.

研究设计

研究类型
Observational
观察模型
Cohort

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Age: above eighteen years and below 60
  • Detectable HCV RNA in serum by PCR
  • ALT level ranged from normal to three fold elevation.
  • Minimum hematological values of hemoglobin of 10.5 g/dl for females, 12g/dl for males; white blood count 3×109/L; platelet counts not less than 100,000/mm
  • Bilirubin, albumin, prothrombin time and creatinine within normal limits.
  • A suitable method for assessment of fibrosis lik liver biopsy or fibroscan will be done before the start of treatment to assess the degree of necroinflammatory response to HCV, which was further subgrouped by HAI scoring system into mild, moderate & severe.

排除标准

  • Decompensated cirrhosis
  • Other causes of liver diseases
  • Autoimmune disorders
  • Uncontrolled diabetes
  • Thyroid dysfunction
  • Neurological or cardiovascular disease
  • Malignancy

结局指标

主要结局

Assess the response to the Interferon therapy.

时间窗: After 72 weeks of the start of therapy of each patient

次要结局

  • Predictors of response to therapy(at the end of the study)

研究者

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

Zekri AR

Proffesor

Cairo University

研究点 (1)

Loading locations...

相似试验