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临床试验/NCT05793970
NCT05793970招募中不适用

Evaluation of IL-6 Levels on Umbilical Cord

Parma University Hospital2 个研究点 分布在 1 个国家目标入组 450 人开始时间: 2022年3月25日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
450
试验地点
2
主要终点
IL6 Levels

研究概览

简要总结

Fetal inflammatory response syndrome (FIRS) is a major cause of non-hypoxic fetal intrapartum injury. One of the most common determinants of FIRS during labor is the exposure to an ongoing intra-amniotic infectious agent as in the event of a chorioamnionitis. Interleuchine-6 (IL-6) is considered a reliable hallmark of FIRS. No specific fetal heart rate pattern for the diagnosis of FIRS have been described so far at intrapartum Cardiotocography (CTG). The aim the present study is to investigate the correlation between intrapartum CTG findings and IL-6 levels on the arterial cord.

详细描述

The labor will be managed according to the local protocol and 5mL of blood will collected from the umbilical artery soon after birth to determine the IL-6 values. CardioTocography (CTG) traces will be retrospectively reviewed by two expert operators that will be blinded to the IL-6 results and will categorize them as "inflammatory" or "not inflammatory".

Inflammatory pattern will be defined in presence of 1) inappropriately high FHR for the given gestational age and/or 2) an increase >10% compared with the FHR baseline values at admission without preceding deceleration with/without reduced variability or absent cycling.

The association between CTG findings as the umbilical levels of IL6 will be analyzed.

研究设计

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

入排标准

年龄范围
18 Years 至 50 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • singleton pregnancies at term submitted to a continuous CTG tracing during labor

排除标准

  • elective Cesarean Delivery, maternal tachycardia or pyrexia >38°C, drugs assumption

结局指标

主要结局

IL6 Levels

时间窗: IL6 will be measured on the umbilical blood sampled within 5 minutes after birth

correlation between intrapartum CTG findings and IL-6 levels on the arterial cord

次要结局

未报告次要终点

研究者

发起方
Parma University Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Tullio Ghi

Full Professor

Parma University Hospital

研究点 (2)

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