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Completed

NCT Number: NCT03089086

South Australian Meningococcal B Vaccine Herd Immunity Study

To estimate the effect on carriage, all year 10, 11, and 12 students will be offered 4CMenB vaccination in South Australia through schools over the study period with 50% of the students enrolled receiving the vaccine in 2017 and 50% in 2018. In year 10 and 11 students, posterior pharyngeal swabs will be obtained at baseline and 12 months post baseline to estimate the difference in carriage prevalence of all genogroups of N. meningitidis between vaccinated and unvaccinated participants.

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Key information

Age range

14 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Vaccinology & Immunology Research Trials Unit

North Adelaide, South Australia, 5006, Australia

About this study

This cluster randomised controlled study will be conducted in the context of funded 4CMenB vaccine offered to all students in years 10, 11, and 12.

Year 10 and 11 students will undergo baseline and 12 months posterior pharyngeal swabs. Year 12 students will undergo baseline posterior pharyngeal swabs only.

Randomisation will take place at the school level and will be stratified by school size ((<60, 60 to 119, and ≥120 students per year level) and school socio-economic status (SES), as measured by the Index of Community Socio-Educational Advantage (ICSEA); (ICSEA <970, 970 to 1020, >1020) For the purposes of the study a school is defined as an educational institution at which students in years 10, 11, 12 physically attend school during the week. All 260 schools in metropolitan and rural SA will be approached to participate in the study. All schools agreeing to participate will be randomised to 4CMenB vaccine in 2017 or 2018. Students at schools randomised to receive the vaccine at baseline will receive the 4CMenB vaccine in 2017. Students at schools randomised to receive the vaccine at the 12 month posterior pharyngeal swab will receive the 4CMenB vaccine in 2018.

Primary Objectives

  • Estimate the difference in carriage prevalence of disease causing genogroup of N. meningitidis (A, B, C, W, X, Y) following the 12 month pharyngeal swab in year 10 and 11 students who received two doses of Bexsero®, compared to unvaccinated students.

Secondary objectives

  • Estimate the difference in carriage prevalence of each disease causing genogroup of N. meningitidis (A, B, C, W, X, Y) following the 12 month pharyngeal swab in year 10 and 11 students who received two doses of Bexsero®, compared to unvaccinated students.
  • Estimate the difference in carriage prevalence of all genogroups of N. meningitidis following the 12 month pharyngeal swab in year 10 and 11 students who received two doses of Bexsero ®, compared to unvaccinated students.
  • Estimate the difference in acquisition (negative at baseline, positive at 12 month followup) of carriage of disease causing genogroups of N. meningitidis (A, B, C, W, X, Y) over a 12 month period in students who received two doses of Bexsero ®, compared to unvaccinated students.
  • Estimate the difference in acquisition (negative at baseline, positive at 12 month followup) of carriage of all genogroups of N. meningitidis over a 12 month period in students who received two doses of Bexsero ®, compared to unvaccinated students
  • Identify characteristics associated with carriage prevalence of all genogroups N. meningitidis in South Australian school students at baseline and 12 months.
  • Identify characteristics associated with carriage prevalence of disease causing genogroups of N. meningitidis (A, B, C, W, X, Y) in South Australian school students at baseline and 12 months.

Exploratory objectives

  • Describe changes in invasive meningococcal rates (attack rates) across all age groups pre and post 4CMenB vaccine intervention in South Australia.
  • Describe N. meningitidis carriage density in year 10, 11, and 12 students using qPCR at baseline and 12 months in both vaccinated and unvaccinated students.
  • Describe genome sequencing of N. meningitidis disease causing (A, B, C, W, X, Y) sequence types in year 10, 11, and 12 students at baseline and at 12 months.
  • In schools randomized to Group A, describe the association of carriage prevalence of disease causing genogroups and vaccine uptake at school level following implementation.
  • In schools randomized to Group A, describe the association of carriage prevalence of all N. meningitidis and vaccine uptake at school level following implementation.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • South Australian secondary school students in years 10, 11, and 12 in 2017
  • Written parental consent for those under the age of 18
  • Written student consent assent for those under the age of 18 (or if 18 years old and older consent for themselves)
  • Available at school for at least the first pharyngeal swab and willing to comply with study procedures

Exclusion criteria

  • Previous anaphylaxis following any component of Bexsero vaccine
  • Previous receipt of meningococcal B vaccine (Bexsero)
  • Known pregnancy

Treatment and study plan

Licensed 4CMenB vaccine

Biological

Two doses (0.5 mL each) of Bexsero ® vaccine at least 1 month to <3 months apart in adolescents.

Other names: Bexsero®

Primary outcomes

  1. Prevalence of all disease causing genogroups of N. meningitidis (A, B, C, W, X, Y)

    Time frame: 12 months

    As measured by PCR at 12 months in vaccinated and unvaccinated year 10 and 11 school students

Secondary outcomes

  1. Prevalence of each N. meningitidis genogroup (A, B, C, W, X, Y)

    Time frame: 12 months

    As measured by PCR at the 12 month pharyngeal swab in vaccinated and unvaccinated year 10 and 11 school students

  2. Prevalence of all N. meningitidis genogroups

    Time frame: 12 months

    As measured by PCR at the 12 month pharyngeal swab in vaccinated and unvaccinated year 10 and 11 school students

  3. Acquisition of disease causing N. meningitidis (A, B, C, W, X, Y) genogroups (negative at baseline, positive at 12 month followup)

    Time frame: 12 months

    As measured by PCR in vaccinated and unvaccinated year 10 and 11 school students

  4. Acquisition of all N. meningitidis

    Time frame: 12 months

    As measured by PCR in vaccinated and unvaccinated year 10 and 11 school students

  5. Risk factors associated with carriage prevalence of all N. meningitidis

    Time frame: Baseline and 12 months

    As measured by PCR at baseline and 12 months

  6. Risk factors associated with carriage prevalence of disease causing N. meningitidis

    Time frame: Baseline and 12 months

    As measured by PCR at baseline and 12 months

Other outcomes

  1. Age specific IMD attack rates

    Time frame: Prior to and following implementation of the intervention

    Age specific IMD attack rates (per 100,000 population) in all age groups in South Australia

  2. Carriage density of N. meningitidis (all genogroups)

    Time frame: Baseline and 12 months

    as measured by qPCR in year 10, 11 and 12 school students at baseline and 12 months

  3. Description of whole genome sequences of carriage isolates

    Time frame: Baseline and 12 months

    Description of whole genome sequences of isolates known to cause disease (serogroup B, W, Y, C)

  4. Whole genogroup sequencing of all carriage isolates

    Time frame: Baseline and 12 months

    Description of whole genome sequences of isolates

  5. Vaccine uptake and carriage prevalence of all N. meningitidis.

    Time frame: 12 months

    Carriage prevalence as measured by PCR

  6. Vaccine uptake and carriage prevalence of disease causing N. meningitidis.

    Time frame: 12 months

    Carriage prevalence as measured by PCR

Sponsors and collaborators

Lead sponsor

University of Adelaide

Other

Collaborators

  • SA Health

Registry information

Acronym: B Part of It

Important dates

Study start
2017
Primary completion
2018
Study completion
2018
First posted
Mar 24, 2017
Registry last updated
Jul 2, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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