Actively Recruiting

Age: 0 - 17Years
All Genders
NCT06761261

Acute Hepatitis in Pediatrics

Led by IRCCS Azienda Ospedaliero-Universitaria di Bologna · Updated on 2025-01-07

437

Participants Needed

2

Research Sites

271 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study aims to investigate wich symptoms and blood test characteristics acute hepatitis manifests in pediatric age. The study will be conducted because acute hepatitis is not an easily and clearly recognized disease in children. This study aims to better characterize this disease by describing the frequency of the different symptoms with which it can manifest and the changes it causes in blood tests. It also aims to assess the occurrence of any complications of pediatric acute hepatitis. The study is observational, so it is limited to collecting data and analyzing the patient's clinical course without interfering with normal clinical practice.

CONDITIONS

Official Title

Acute Hepatitis in Pediatrics

Who Can Participate

Age: 0 - 17Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 0 and 17 years (extremes included)
  • Access to Pediatric Emergency Room and/or hospitalization
  • Diagnosis of acute hepatitis
Not Eligible

You will not qualify if you...

  • Parent or guardian refuses to participate in the study
  • Mild hypertransaminasemia (less than 5 times the upper limit of normal) in a patient with known chronic liver dysfunction such as liver cirrhosis
  • Neonatal jaundice without hepatocyte involvement or signs of cholestasis (presence of indirect bilirubin with normal AST, ALT, and GGT)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

Azienda USL di Bologna Ospedale Maggiore

Bologna, Italy, 40124

Actively Recruiting

2

IRCCS Azienda Ospedaliero - Universitaria di Bologna

Bologna, Italy, 40138

Actively Recruiting

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Research Team

A

Arianna Dondi

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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