Parvovirus B19 in pregnancy and its effects on the baby

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

Researchers will collect clinical data from pregnant women over 18 with confirmed parvovirus B19 infection and from their neonates to determine the rate of intrauterine transmission and fetal/newborn complications. The study will record maternal risk factors, pregnancy outcomes, management interventions, and longer-term sequelae in infants. Data will be gathered at participating hospitals in Lombardy, Italy, and analyzed to identify factors associated with worse outcomes and to evaluate the effectiveness of current management approaches. As an observational registry, no experimental treatments are assigned.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Pregnant women \>18 years with parvovirus B19 infection and their neonates.

Exclusion Criteria:

* None

Where it's running

• Fondazione IRCCS Policlinico San Matteo
  Pavia, Lombardy, Italy Recruiting
• Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico
  Milan, Italy Recruiting
• ASST Fatebenefratelli Sacco
  Milan, Italy Recruiting
• ASST degli Spedali Civili di Brescia
  Brescia, Italy Not yet recruiting
• Fondazione IRCCS San Gerardo dei Tintori
  Monza, Italy Not yet recruiting

Study contacts

• Study coordinator: Daniele Lilleri
• Email: d.lilleri@smatteo.pv.it
• Phone: +39 0382 502420

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.