跳至主要内容
临床试验/CTIS2022-500714-25-01
CTIS2022-500714-25-01招募中1 期

Congenital CMV treated with valaciclovir during pregnancy: a prospective cohort study

Z Leuven0 个研究点目标入组 112 人开始时间: 2023年7月5日最近更新:
适应症

试验速览

阶段
1 期
状态
招募中
发起方
入组人数
112

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

年龄范围
In Utero 至 64(—)

入选标准

  • Voluntary written informed consent of the participant or their legally authorized representative has been obtained prior to any screening procedures, 18 years or older, Proven first trimester primary CMV infection

排除标准

  • Participant has a history of kidney function problems, liver function problems, immunocomprimised, Any disorder, which in the Investigator’s opinion might jeopardise the participant’s safety or compliance with the protocol, Any prior or concomitant treatment(s) that might jeopardise the participant’s safety or that would compromise the integrity of the Trial, Participation in an interventional Trial with an investigational medicinal product (IMP) or device

研究者

发起方
Z Leuven

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