Protection Against Pneumococcal Infection in Children With T1DM
NCT ID: NCT01939522
Last Updated: 2017-05-09
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
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COMPLETED
PHASE4
50 participants
INTERVENTIONAL
2013-08-31
2017-01-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
PREVENTION
NONE
Study Groups
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Prevenar13® (13-valent pneumococcal conjugate vaccine)
Prevenar13 administered as a single dose, 0.5ml Intramuscular liquid form intervention at baseline.
13-valent pneumococcal conjugate vaccine (PCV13)
Interventions
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13-valent pneumococcal conjugate vaccine (PCV13)
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Aged between 6 years and 17 years.
* Parent/legal guardian willing and able to give informed consent.
* No previous immunisation with a pneumococcal conjugate vaccine (PCV).
* Willing to allow the General Practitioner to be notified of participation in the study.
Exclusion Criteria
* Bleeding diathesis or condition associated with prolonged bleeding time that would contraindicate intramuscular injection.
6 Years
17 Years
ALL
No
Sponsors
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University of Oxford
OTHER
Responsible Party
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Locations
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Oxford University Hospitals NHS Trust
Oxford, Oxfordshire, United Kingdom
Countries
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Other Identifiers
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2013-001024-19
Identifier Type: EUDRACT_NUMBER
Identifier Source: secondary_id
OVG 2013/03
Identifier Type: -
Identifier Source: org_study_id
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