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临床试验/NCT07086144
NCT07086144招募中不适用

Efficacy of a Myocardial Panel (Virological, Bacterial and Autoimmune) in the Management and Treatment of Pediatric Myocarditis Complicated With Arrhythmias or Ventricular Dysfunction

Azienda Ospedaliero, Universitaria Ospedali Riuniti2 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2024年1月1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
30
试验地点
2
主要终点
Arrhythmias duration

研究概览

简要总结

The goal of this observational study is to determine the efficacy a of combined management and treatment driven by the systematic determination of viral genome, bacterial serology, and markers of inflammation in pediatric patients (< 18 years old) diagnosed with myocarditis complicated by arrhythmias (supraventricular and ventricular tachycardias and heart block) or ventricular dysfunction (left ventricular ejection fraction < 50% or right ventricular fractional area change < 35%).

The main question it aims to answer is: Does this panel help resolve arrhythmias or myocardial dysfunction due to myocarditis during hospitalisation and follow-up?

Researchers will compare patients managed and treated in 2024 without applying the myocarditis panel with those enrolled in 2025 who received the panel. Arrhythmias and myocardial dysfunction will be managed in accordance with recent guidelines. Antiviral, antibiotic or immunosuppressive therapies will be implemented in addition to standard therapy when required by the panel.

详细描述

The Investigators will enrol consecutive pediatric patients (< 18 years old) presenting with myocarditis complicated by arrhythmias or ventricular dysfunction.

The participants will undergo routine daily visits and electrocardiographic and echocardiographic assessment during hospitalisation (within 8 weeks).

During follow-up, a routine visit including an echocardiogram, ECG, and blood tests (complete blood count, liver function tests, renal function tests, inflammation indices, and myocardial necrosis tests) will be performed within the first 40 days of discharge; thereafter, every 3 months after discharge for a total of 6 months of follow-up.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Crossover
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • All the consecutive pediatric patients (< 18 years old) presenting with myocarditis complicated by arrhythmias or myocardial dysfunction

排除标准

  • Refused consent to be included in the study given by parents or legal tutors
  • Uncomplicated myocarditis presenting without arrhythmias or myocardial dysfunction

结局指标

主要结局

Arrhythmias duration

时间窗: From enrollment to the end of the hospitalisation (maximum of 8 weeks)

Total duration of in-hospital arrhythmias assessed by electrocardiography

Myocardial dysfunction

时间窗: From enrollment to the end of the hospitalisation (maximum of 8 weeks)

Total duration of myocardial dysfunction assessed by echocardiography

次要结局

  • Follow-up(6 months)

研究者

发起方
Azienda Ospedaliero, Universitaria Ospedali Riuniti
申办方类型
Other
责任方
Principal Investigator
主要研究者

Francesco Bianco

Principal investigator

Azienda Ospedaliero, Universitaria Ospedali Riuniti

研究点 (2)

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