跳至主要内容
临床试验/NCT06694428
NCT06694428招募中不适用

Evaluation of Software for Interpreting Virological Results Indicated for the Diagnosis of Cytomegalovirus (CMV) Infection During Pregnancy and Intended for Health Professionals

Assistance Publique - Hôpitaux de Paris5 个研究点 分布在 1 个国家目标入组 491 人开始时间: 2025年4月4日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
491
试验地点
5
主要终点
Evaluation of the detection rate of primary CMV infection in the first trimester of pregnancy using the MyCMV tool

研究概览

简要总结

Congenital cytomegalovirus (CMV) infection is the most common congenital infection with a birth prevalence of 0.4% in Europe. It is the leading non-genetic cause of sensorineural hearing loss and a major cause of neurodevelopmental disabilities. The risk of intrauterine transmission is highest when primary infection occurs during pregnancy. Primary CMV infection is asymptomatic or causes non-specific symptoms and only serology can diagnose it with certainty.

The diagnosis of CMV infection is based on the combination of 2 or 3 serological markers and the interpretation of the results is more complex than for other infections and may require additional analyses and sometimes delay the diagnosis and the implementation of secondary prevention of CMV transmission to the fetus by the administration of valaciclovir. Indeed, the effectiveness of secondary prevention is conditioned by the early administration of treatment after the maternal primary infection.

The National Reference Center for Congenital CMV Infections at Necker Hospital, in collaboration with the virology laboratory at Paul Brousse Hospital, has developed the MyCMV "expert" tool, which is a decision-making algorithm that allows the interpretation of CMV serology and CMV PCR results.

The hypothesis of the study is that the use and provision of this MyCMV "expert" tool to health professionals (biologists, midwives and obstetricians) for the interpretation of virological results could avoid a delay in diagnosis and would allow patients to be referred more quickly to a prenatal diagnosis center for appropriate management of CMV infection.

The aim of the study is to evaluate the rate of detection of primary CMV infection in the first trimester of pregnancy using the MyCMV tool compared with the reference method (results interpreted by the centre's expert investigator).

详细描述

Congenital cytomegalovirus (CMV) infection is the most common congenital infection with a birth prevalence of 0.4% in Europe. It is the leading non-genetic cause of sensorineural hearing loss and a major cause of neurodevelopmental disabilities. The risk of intrauterine transmission is highest when primary infection occurs during pregnancy. Primary CMV infection is asymptomatic or causes non-specific symptoms and only serology can diagnose it with certainty.

The diagnosis of CMV infection is based on the combination of 2 or 3 serological markers and the interpretation of the results is more complex than for other infections and may require additional analyses and sometimes delay the diagnosis and the implementation of secondary prevention of CMV transmission to the fetus by the administration of valaciclovir. Indeed, the effectiveness of secondary prevention is conditioned by the early administration of treatment after the maternal primary infection.

The National Reference Center for Congenital CMV Infections at Necker Hospital, in collaboration with the virology laboratory at Paul Brousse Hospital, has developed the MyCMV "expert" tool, which is a decision-making algorithm that allows the interpretation of CMV serology and CMV PCR results.

The hypothesis of the study is that the use and provision of this MyCMV "expert" tool to health professionals (biologists, midwives and obstetricians) for the interpretation of virological results could avoid a delay in diagnosis and would allow patients to be referred more quickly to a prenatal diagnosis center for appropriate management of CMV infection.

The aim of the study is to evaluate the rate of detection of primary CMV infection in the first trimester of pregnancy using the MyCMV tool compared with the reference method (results interpreted by the centre's expert investigator). We also aim to evaluate the dating of the maternal primary infection in weeks of amenorrhoea and additional tests given by the MyCMV tool compared with the reference method.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Other

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Pregnant woman
  • And for whom a CMV serology including the search for CMV IgG and IgM antibodies is prescribed at the Necker-Enfants Malades or Paul Brousse hospital or CHU Limoges
  • And with positive anti-CMV IgM or in the grey zone of the technique
  • And for whom the date of start of pregnancy is known
  • And who does not object to the use of their data in the context of this research

排除标准

  • 未提供

研究组 & 干预措施

Patients

Pregnant women with prescription of a CMV serology including the search for CMV IgG and IgM antibodies, care at the Necker-Enfants Malades, Paul Brousse hospitals, or the CHU Limoges, with positive CMV IgM antibodies or in the grey zone of the technique and for whom the date of start of pregnancy is known.

干预措施: Reinterpretation of CMV serology results using the MyCMV tool on the basis of the serology results performed (Other)

结局指标

主要结局

Evaluation of the detection rate of primary CMV infection in the first trimester of pregnancy using the MyCMV tool

时间窗: Time 0

Detection of primary CMV infection in the first trimester of pregnancy by the MyCMV tool or by the reference method. In the context of this study, the reference method is the interpretation of the results by the expert investigator of the center, without using the MyCMV tool.

次要结局

  • Dating in weeks of amenorrhea of the date of primary infection by the MyCMV tool and by the reference method(Time 0)
  • Recommendations for the conduct to be adopted for carrying out additional analysis by the MyCMV tool(Time 0)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (5)

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