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CompletedNCT03407690PIN2Updated Aug 29, 2019

A Study to Assess the Carriage of Pneumococci in Children Aged ≤8 Years, and Their Household Contacts

An observational study in Immunization; Infection, sponsored by Public Health England. Completed at 2 sites in United Kingdom. Per ClinicalTrials.gov, last updated 2019-08-29.

Sponsored by Public Health England · Observational

Study type
Observational
Model
Family-based
Time perspective
Prospective
Enrollment
280
Sex
All
01

Study summary

Since the introduction of pneumococcal conjugate vaccines, this research group has conducted several carriage studies. These were at key points in the evolution of the pneumococcal immunisation schedule, with regard to the introduction of PCV7, the change to PCV13 and the impending change in number of doses of PCV13 given to infants. The last carriage study, conducted in 2015/16 identified interesting changes in carriage patterns which will further be explored by the current planned study.

Nasopharyngeal swabs and saliva swabs will be taken from healthy subjects and any pneumococci present will be cultured and serotyped using standard methods, as per our previous studies (Hussain et al., 2005; Flasche et al., 2011; van Hoek et al., 2014).

Read the detailed description

Streptococcus pneumoniae frequently colonises the human nasopharynx and most carriers remain asymptomatic. However, sometimes the organism may spread locally to cause non-invasive, mucosal infections such as sinusitis and otitis media or may invade the bloodstream and cause serious infections, including septicaemia, meningitis and pneumonia. In the 2005/06 epidemiological year, there were 6,391 cases of invasive pneumococcal diseases in England and Wales, with the highest incidence in the first year of life. The risk of developing invasive disease is dependent on both the susceptibility of the host and the invasiveness of the pneumococcus, which is largely determined by the characteristics of its polysaccharide capsule. Of the >90 known pneumococcal serotypes, the seven serotypes (4, 6B, 9V, 14, 18C, 19F and 23F) included in the 7-valent pneumococcal conjugate vaccine (PCV7) accounted for around 75% of childhood IPD cases in England and Wales prior to routine pneumococcal vaccination.

There have been several carriage studies conducted by this group at key points in the evolution of the pneumococcal vaccination policy of the UK, before use of any PCV, once the PCV7 had been introduced and once the change to PCV13 had been made. Studies have shown that conjugate vaccines, of which PCV7 and PCV13 are examples, can affect carriage of the bacteria against which the vaccinate. This series of carriage studies is important in understanding which pneumococcal strains are in the nose and so are potentially part of the chain of transmission as the vaccinations given have changed. For pneumococcus, where there are many strains, it is important to understand whether clearing carriage of a strain contained in the vaccine creates a niche which can be exploited by a strain of greater virulence or one which causes more serious disease. Our last such study suggested there are changes which we should continue to monitor, which is why the current study is now happening.

Nasopharyngeal swabs and saliva swabs will be taken from healthy subjects and any pneumococci present will be cultured and serotyped using standard methods, as per our previous studies.

02

Conditions studied

  • Immunization; Infection
03

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

  • At least 200 children (index cases) aged ≤8 years and at least 200 household contacts.

Inclusion criteria

  1. At least one child aged ≤8 years in the household
  2. Written informed consent obtained from the child's parent / legal guardian for their participation, and for any participating household contacts

Exclusion criteria

Exclusion Criteria:

  • Moderate to severe cerebral palsy or other debilitating condition
  • Syndromes and neurological disorders affecting swallowing.
  • Ear, nose \& throat disorders affecting local anatomy for swabbing (e.g. malformed ears)
  • Confirmed or suspected immunodeficiency (congenital or acquired) or receiving immunosuppressive therapy.
04

Study design

Observational model
Family-based
Time perspective
Prospective
Enrollment
280 participants (actual)
Patient registry
No
Biospecimen retention
Samples without dna

Groups and cohorts

  • PIN2 study participants

    All those giving swabs for the study

    Other: nasal swab

Interventions

  • Othernasal swab

    collection of nasal swab to allow carriage of pneumococci to be assessed

05

What researchers measure

Primary outcomes

  1. pneumococcal carriage rates

    pneumococcal carriage rates for PCV13 and non-PCV13 serotypes in children and infants eligible for primary or booster immunisation with PCV 13 and their household contacts

    Time frame: through study completion, expected 6 months

06

Study locations

2 sites
  • Gloucestershire Primary Care
    Gloucester, Gloucestershire, United Kingdom
  • Hertfordshire primary care
    Hertford, Hertfordshire, United Kingdom
07

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT03407690
Lead sponsor
Public Health England
Responsible party
Sponsor
First posted
Jan 23, 2018
Start date
Feb 14, 2018
Primary completion
Jul 31, 2018
Completion
Jul 31, 2018
Last update
Aug 29, 2019

Study contacts

Elizabeth Coates, PhD
study director · Public Health England

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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