STORM: A Surveillance Study on Timing and Coverage Of Rotavirus and MenB Vaccine Co-administration in Campania Region, Italy

Sponsor
Federico II University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05212935
Collaborator
Merck Sharp & Dohme LLC (Industry)
2,000
11

Study Details

Study Description

Brief Summary

A two-phases study will be carried out with the following aims

  1. st phase (2018-2020)
  • To investigate the vaccination coverage for Rotavirus vaccine (RV) in Campania Region together with other pediatric vaccinations scheduled in the first 12 months of life: hexavalent, pneumococcal conjugate (PCV), meningococcal B (MenB)

  • To collect data on appropriate timing of the 3 doses of human bovine pentavalent reassortant vaccine (RV5) administration

  • To evaluate the frequency of a co-administration of RV5 with other vaccines scheduled in the first 12 months of life (hexavalent/PCV+RV5, MenB+RV5 vs RV5 alone) and assess the variability in co-administration rates according to RV5 dose

  1. nd phase (2020-2022)
  • To investigate the effect of Coronavirus-Disease-19 (COVID-19) pandemic on vaccination coverage in the first year of life, focusing on RV vaccination

  • To investigate the effect of COVID-19 pandemic on timing of vaccine administration in the first year of life, focusing on those vaccines without catch-up vaccination schedule (i.e. RV)

Hypothesis are the following:
  • Vaccination coverage and timing of vaccines scheduled in the first year of life are not fully aligned with what is established by the Italian National Prevention Plan 2017-2019

  • Co-administration of RV5 and MenB in comparison with other coadministration e.g. hexavalent/PCV is lower

  • Co-administration of RV5 and MenB allows to ensure appropriate timing of RV vaccination schedule

  • COVID-19 pandemic may have affected the overall vaccination coverage as well as the timing of selected vaccination scheduled in the first year of life, with a more relevant impact on vaccines for whom a catch-up vaccination schedule is not feasible, such as RV immunization.

Condition or Disease Intervention/Treatment Phase
  • Biological: Rotavirus Vaccine

Detailed Description

The study will be carried out in collaboration with eight Vaccination Centers, which are responsible in Italy for the organization and delivery of vaccination as well as for overseeing implementation of vaccinations and monitoring coverage, in four provinces of

Campania Region (representative of different regional areas) with the following aims:
  • To investigate the vaccination coverage for Rotavirus vaccine (RV) in Campania Region together with other pediatric vaccinations scheduled in the first 12 months of life: hexavalent, pneumococcal conjugate (PCV), meningococcal B (MenB)

  • To collect data on appropriate timing of the 3 doses of human bovine pentavalent reassortant vaccine (RV5), which is the most used RV vaccine in Campania Region.

  • To evaluate the frequency of a co-administration of RV5 with other vaccines scheduled in the first 12 months of life (hexavalent/PCV+RV5, MenB+RV5 vs RV5 alone) and assess the variability in co-administration rates according to RV5 dose

  • To investigate the effect of Coronavirus-Disease-19 (COVID-19) pandemic on vaccination coverage and on timing of vaccine administration in the first year of life, focusing on RV vaccination

The study consists of two parallel phases:
  1. First phase aimed at enrolling children who received a vaccine in first 12 months of life between January 2018 and December 2020. These data would provide informative data about the pre-pandemic situation and the impact of restrictive measures against COVID-19 on vaccination.

  2. Second phase, enrolling children aged between 6 weeks to 12 months who will enter the national Immunization schedule according to the Italian Immunization Plan up to June 2022 (cohort 2021), in order to investigate a possible role of COVID-19 pandemic and new strategies applied at local level for a catch-up vaccination in the first year of life.

A specific digital dataset will be created to collect data about the number of eligible children who received vaccinations in the territory of each Vaccination Center during the study period. The rough data will be extrapolated by an investigator for each Vaccination province through a single chart reviewing from the regional vaccination database. The regional electronic immunization register is currently used for the entire immunization process (from vaccination call-out, to calculating the vaccination coverage, up to send aggregated data to the Ministry of Health in order to estimate the national vaccination coverage).

The characteristics of each vaccine administered will be recorded (i.e. brand, number of doses) as well as the lass of time between vaccination and possible delay.

Anonymized data obtained by the Regional Registry will be used to analyze vaccination coverage according to age and cohort, timing of administration and frequency and type of co-administration.

Hypothesis are the following:
  • Vaccination coverage and timing of vaccines scheduled in the first year of life are not fully aligned with what is established by the Italian National Prevention Plan 2017-2019

  • Co-administration of RV5 and MenB in comparison with other coadministration e.g. hexavalent/PCV is lower

  • Co-administration of RV5 and MenB allows to ensure appropriate timing of RV vaccination schedule

  • COVID-19 pandemic may have affected the overall vaccination coverage as well as the timing of selected vaccination scheduled in the first year of life, with a more relevant impact on vaccines for whom a catch-up vaccination schedule is not feasible, such as RV immunization.

Study Design

Study Type:
Observational
Anticipated Enrollment :
2000 participants
Observational Model:
Ecologic or Community
Time Perspective:
Retrospective
Official Title:
A Surveillance Study on Timing and Coverage Of Rotavirus and MenB Vaccine Co-administration in Campania Region, Italy
Anticipated Study Start Date :
May 1, 2022
Anticipated Primary Completion Date :
Oct 1, 2022
Anticipated Study Completion Date :
Apr 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Children below 12 months of age receiving vaccines according to the National Vaccination Plan

All children who received vaccination in their first 12 months of life between January 2018 and June 2022 in the Regional Vaccination Centers involved in the study. Children will be classified in sub-groups, according to different vaccination schedules (single or co-administration) and order of vaccine uptake.

Biological: Rotavirus Vaccine
administration of the 3 doses of Rotavirus human bovine pentavalent reassortant vaccine

Outcome Measures

Primary Outcome Measures

  1. Overall proportion of children fully immunized for RV and proportion of immunized children in each subgroup [32 weeks]

  2. Proportion of children receiving the first RV5 dose within 12 weeks of age [32 weeks]

  3. Proportion of children completing RV5 schedule within 32 weeks of age [32 weeks]

  4. Proportion of children receiving the co-administration RV5 + MenB [32 weeks]

Secondary Outcome Measures

  1. Proportion of children partially immunized (1 or 2 doses) or not immunized for RV in each subgroup [32 weeks]

  2. Proportion of children receiving RV5 immunization doses alone [32 weeks]

  3. Proportion of children receiving the co-administration of RV5+hexavalent/PCV [32 weeks]

Eligibility Criteria

Criteria

Ages Eligible for Study:
6 Weeks to 12 Months
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • all children receiving vaccination according to the Italian National Vaccine Prevention Plan 2017-2019
Exclusion Criteria:
  • primary outcomes data missing.

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Federico II University
  • Merck Sharp & Dohme LLC

Investigators

  • Principal Investigator: Andrea Lo Vecchio, MD, PhD, Federico II University

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Andrea Lo Vecchio, MD, PhD, Assistant Professor, Federico II University
ClinicalTrials.gov Identifier:
NCT05212935
Other Study ID Numbers:
  • 432/21
First Posted:
Jan 28, 2022
Last Update Posted:
Mar 17, 2022
Last Verified:
Mar 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Andrea Lo Vecchio, MD, PhD, Assistant Professor, Federico II University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 17, 2022