A Study to Assess the Carriage of Pneumococci in Children Aged 1-5 Years, and Their Household Contacts
NCT ID: NCT02522546
Last Updated: 2019-03-22
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
400 participants
OBSERVATIONAL
2015-07-31
2016-12-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Pneumococcal vaccines (PCV) have been given in the national immunisation schedule since 2006.Carriage studies allow assessment of how the strains in the nose change over time, in that by clearing some strains away which other strains take up those niches in their place both in children and in their close/household contacts. This helps to inform the best use of the vaccines available and for future vaccine development and which strains would be useful to include.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
A Study to Assess the Carriage of Pneumococci in Children Aged ≤8 Years, and Their Household Contacts
NCT03407690
A Study to Assess the Impact of Pneumococcal Conjugate Vaccination Programme on the Carriage of Pneumococci
NCT01040143
Understanding Pneumococcal Carriage and Disease 2017-2020
NCT03102840
Understanding Pneumococcal Carriage and Disease
NCT01996007
Long-term Impact of Pneumococcal Conjugate Vaccine on Carriage
NCT00294021
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
This group has conducted three previous carriage studies, and this will be the fourth. The first was before any vaccine was used, the second just after PCV7 was introduced and the third after the UK moved to using PCV13. These carriage studies allow assessment of how the strains in the nose change over time, in that by clearing some strains away which other strains take up those niches in their place both in children and in their close/household contacts. This helps to inform the best use of the vaccines available and for future vaccine development and which strains would be useful to include.
All families registered at participating surgeries, with a child aged 1-5 years, will be invited to take part. The study involves a single nasopharyngeal swab and a saliva swab from the child and as many other household members as are happy to participate. Participants may be seen at their GP surgery or in the home if more mutually convenient
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
nasopharyngeal swab
Children ages 1-5 years and their household contacts
nasopharyngeal swab
nasopharyngeal swab
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
nasopharyngeal swab
nasopharyngeal swab
Other Intervention Names
Discover alternative or legacy names that may be used to describe the listed interventions across different sources.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Written informed consent obtained from the child's parent / legal guardian for their participation, and for any participating household contacts
Exclusion Criteria
* 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.
1 Year
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Public Health England
OTHER_GOV
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Prof. Elizabeth Miller
Prof Elizabeth Miller
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Elizabeth Coates, PhD
Role:
Public Health England
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Gloucestershire primary care
Gloucestershire, Gloucestershire, United Kingdom
Hertfordshire primary care
Hertfordshire, Hertfordshire, United Kingdom
Countries
Review the countries where the study has at least one active or historical site.
References
Explore related publications, articles, or registry entries linked to this study.
Southern J, Andrews N, Sandu P, Sheppard CL, Waight PA, Fry NK, Van Hoek AJ, Miller E. Pneumococcal carriage in children and their household contacts six years after introduction of the 13-valent pneumococcal conjugate vaccine in England. PLoS One. 2018 May 25;13(5):e0195799. doi: 10.1371/journal.pone.0195799. eCollection 2018.
Related Links
Access external resources that provide additional context or updates about the study.
Published study results
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
PIN
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.