EUCTR2011-005378-44-NL进行中（未招募）不适用
CONgenital Cmv: Efficacy of antiviral treatment in a Randomized controlled Trial - CONCERT
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
- MC
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
- All
入选标准
- •Infants with congenital CMV infection, and hearing loss (=20 dB, in one or both ears).
- •Age at time of inclusion is < 12 weeks after birth.
- •>37 weeks gestational age.
- •Birth weight >2500 gram.
- •Parental signed informed consent.
- •Are the trial subjects under 18? yes
- •Number of subjects for this age range: 50
- •F.1.2 Adults (18-64 years) no
- •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
- •Indications for symptomatic congenital CMV infection based on diagnostics carried out prior to the inclusion of the child in the trial.
- •In case during the house visit the presence of a symptomatic CMV infection is doubted, inclusion will be discussed. Depending on the medical history taking, physical examination and laboratory tests inclusion will be decided upon.
- •Treatment with other antiviral agents or immunoglobulins.
- •Leucopenia < 0,5 x 10*9/L (blood sample tested at t=0).
研究者
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