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Evaluation of the Effect of Nirsevimab on Hospitalizations Due to RSV Infection in Infants Under One Year of Age.

Recruiting
Conditions
Respiratory Synctial Virus Infections
Interventions
Registration Number
NCT06856967
Lead Sponsor
Meyer Children's Hospital IRCCS
Brief Summary

This study aims to evaluate the impact of Nirsevimab, a monoclonal antibody used for RSV prophylaxis, on reducing RSV- related hospitalizations. It will be conducted at 8 pediatric departments in Tuscany, Italy. First, a matched case-control study investigates the real-world effectiveness of Nirsevimab in preventing RSV-related lower respiratory tract infection (LRTI) hospitalizations during the RSV epidemic season 2024-2025. Second, a descriptive study examines how the Nirsevimab immunization campaign affects RSV epidemiology, focusing on patients' age, comorbidities, infection severity, and clinical outcomes. The findings aim to optimize RSV prevention strategies and inform public health policies.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
138
Inclusion Criteria

Case patients

  • Age <12 months
  • Diagnosis of LRTI (i.e., bronchiolitis and/or pneumonia) at admission
  • Positive RSV PCR on nasopharyngeal swab Control patients
  • Age <12 months
  • Diagnosis of LRTI (i.e., bronchiolitis and/or pneumonia) at admission
  • Hospitalized for conditions other than respiratory infections
Exclusion Criteria
  • Parental refusal
  • Previous immunization with Palivizumab
  • Previous maternal RSV vaccine immunization during pregnancy

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
CasesNirsevimabPatients aged \<1 years hospitalized with confirmed bronchiolitis
ControlsNirsevimabPatients aged \<1 years hospitalized for condition other than confirmed bronchiolitis
Primary Outcome Measures
NameTimeMethod
The proportion of patients immunized with Nirsevimab among children hospitalized for RSV-related LRTI and those in the control group.November 2024-March 2025
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (8)

SOC Pediatria Ospedale Santa Maria Annunziata

๐Ÿ‡ฎ๐Ÿ‡น

Bagno a Ripoli, Firenze, Italy

SOC Pediatria e Neonatologia Ospedale San Jacopo

๐Ÿ‡ฎ๐Ÿ‡น

Pistoia, Italy

SOC Pediatria e Neonatologia Ospedale Santo Stefano

๐Ÿ‡ฎ๐Ÿ‡น

Prato, Italy

SOC Pediatria Ospedale San Donato

๐Ÿ‡ฎ๐Ÿ‡น

Arezzo, Italy

Meyer Children's Hospital IRCCS

๐Ÿ‡ฎ๐Ÿ‡น

Florence, Italy

Azienda Ospedaliero Universitaria Pisana

๐Ÿ‡ฎ๐Ÿ‡น

Pisa, Italy

SOC Neonatologia e Terapia Intensiva Neonatale, Ospedale San Giovanni Di Dio

๐Ÿ‡ฎ๐Ÿ‡น

Firenze, Italy

SOC Pediatria AOU Senese

๐Ÿ‡ฎ๐Ÿ‡น

Siena, Italy

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