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临床试验/EUCTR2008-006560-11-IT
EUCTR2008-006560-11-IT进行中(未招募)不适用

Prevention of human cytomegalovirus (HCMV) mother-to-fetus transmission by administration of virus-specific hyperimmune globulin to pregnant women with primary HCMV infection - ND

OSPEDALE POLICLINICO S. MATTEO0 个研究点开始时间: 2009年2月9日最近更新:
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试验速览

阶段
不适用
状态
进行中(未招募)
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
Female

入选标准

  • pregnant women, >/= 18 years, primary HCMV infection at 5-26 week of gestation, Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • 1)multiple pregnancy, 2)history of HIV infection, 3) known immunodeficiency or immunosuppression, 4) congenital or required auotimmune desease 5) known intollerance to proteins of human origin, 6) hypersensitivity to human immunoglobulin, 7) suspected serious organic or psychiatric desease 8) not willing to give informed consent, not willing to give consent to treatment of personal pseudonymised data.

研究者

发起方
OSPEDALE POLICLINICO S. MATTEO

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