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临床试验/JPRN-UMIN000002580
JPRN-UMIN000002580招募中未知

Prospective validation for the usefulness of Genome-wide association study (GWAS) in predicting the effects of anti-viral therapy on chronic hepatitis C - Chronic hepatitis C and GWAS

Research Center for Hepatitis & Immunology, Kohnodai Hospital, International Medical Center of Japan0 个研究点目标入组 250 人开始时间: 2009年10月8日最近更新:

试验速览

阶段
未知
状态
招募中
发起方
入组人数
250

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
20years-old 至 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1) Patients taking Sho-sai-koto(herbal medicine) 2) Autoimmune hepatitis 3) Patients with history of interstitial pneumonia 4) Patients with previous history of drug allergy against ribavirin, peginterferon alpha2a (Pegasys), peginterferon alpha2b (Pegintron), or other interferons 5) Patients with previous history of drug allergy against biological products such as vaccines 6) Liver cirrhosis, liver failure or hepatocellular carcinoma 7) Patients with the following laboratory data at the start of peginterferon and ribavirin combination therapy: WBC counts less than 4,000/microliter and Neutrophil counts less than 1,500/microliter; Platelets counts less than 90,000/microliter (peginterferon alpha2a) or 100,000/microliter(peginterferon alpha2b); Hemoglobin levelsless than 12g/dL 8) Women who are pregnant or have its possibility 9) Patients who refuse birth control, including male patients whose patners may have the chance to be pregnant 10) Patients whom the physicians in charge judge their enrollment inappropriate

研究者

发起方
Research Center for Hepatitis & Immunology, Kohnodai Hospital, International Medical Center of Japan

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