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临床试验/NCT01226446
NCT01226446已完成2 期

Multicenter Open and Prospective Trial Assessing the Efficacy of Vitamin D Supplementation in Addition to Pegylated Interferon Plus Ribavirin in Null-Responders Patients With Chronic Viral Hepatitis C Genotype 1 or 4

French National Agency for Research on AIDS and Viral Hepatitis2 个研究点 分布在 1 个国家目标入组 32 人开始时间: 2010年11月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
32
试验地点
2
主要终点
Negativity of HCV RNA below 12UI/mL after 12 weeks of antiviral combination therapy

研究概览

简要总结

Vitamin D deficiency is commonly found in patients with chronic hepatitis C. The investigators hypothesize that the correction of hypovitaminosis D before the initiation of anti-HCV combination therapy and the maintenance of an optimal vitamin D status during antiviral therapy could improve the antiviral efficacy

详细描述

An open-label, prospective evaluation of the efficacy of vitamin D supplementation starting 1 month before and continuing for the duration of combination therapy with pegylated interferon alpha (2a or 2b) plus ribavirin in patients with chronic viral hepatitis C genotype 1 or 4, nonresponders to a first antiviral therapy.Vitamin D supplementation is started one month before antiviral therapy in order to introduce pegylated interferon plus ribavirin in patients with optimal vitamin D status

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

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

  • Chronic Hepatitis C Genotype 1 or 4
  • Hypovitaminosis D defined by a value <30 ng / ml
  • Patient non responder to previous antiviral combination therapy of Pegylated Interferon and Ribavirin defined by a decrease in viral load <2 log at week 12 of the first course (Peg/RBV)
  • Patient who received at least 80% of the optimal dose of Pegylated Interferon and Ribavirin according to current recommendations
  • Patient for which the investigating physician decided to initiate treatment for hepatitis C combination therapy

排除标准

  • Decompensated liver disease: Child-Pugh B> 8 or one of the following criteria: bilirubin> 35 micromol/L, TP <50%, ascites, recurrent encephalopathy
  • Positive serology for HBV and HIV
  • Alcohol consumption exceeding 50 g/day
  • Chronic intake of vitamin D
  • Thrombocytopenia <50 000/mm ³, neutropenia <750/mm ³, hemoglobin <11 g/dL
  • Pregnant women

研究组 & 干预措施

Addition of Vitamin D to Peg-interferon plus Ribavirin

Experimental

干预措施: vitamin D (Drug)

结局指标

主要结局

Negativity of HCV RNA below 12UI/mL after 12 weeks of antiviral combination therapy

时间窗: at week 12

次要结局

  • Changes in HCV viral load after correction of vitamin D deficiency (delta log)(at day 0)
  • Changes in HCV viral load (delta log)(at week 12)
  • Negativity of HCV RNA below 12 UI/ml(at week 72)
  • Changes in HCV viral load (delta log)(at week 4)
  • Negativity of HCV RNA below 12 UI/ml(at week 24)

研究者

发起方
French National Agency for Research on AIDS and Viral Hepatitis
申办方类型
Other Gov
责任方
Sponsor

研究点 (2)

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