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Trial registered on ANZCTR
Registration number
ACTRN12614000354684
Ethics application status
Approved
Date submitted
19/03/2014
Date registered
2/04/2014
Date last updated
20/06/2017
Type of registration
Prospectively registered
Titles & IDs
Public title
Targeted enhanced surveillance to observe vaccine impact against Pneumococcus
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Scientific title
Evaluation of the effectiveness of the 13-valent pneumococcal conjugate vaccine against pneumococcal pneumonia in children
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Secondary ID [1]
284253
0
Nil
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Universal Trial Number (UTN)
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Trial acronym
TESTOV-Pneumo
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Pneumonia
291369
0
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Streptococcus pneumoniae
291371
0
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Empyema
291412
0
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Condition category
Condition code
Infection
291735
291735
0
0
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Studies of infection and infectious agents
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Respiratory
291736
291736
0
0
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Other respiratory disorders / diseases
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Public Health
291857
291857
0
0
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Other public health
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Intervention/exposure
Study type
Observational
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Patient registry
False
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Target follow-up duration
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Target follow-up type
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Description of intervention(s) / exposure
Pneumonia caused by Streptococcus pneumoniae is a leading cause of childhood morbidity and mortality. While vaccination programs against pneumococcus are highly effective in reducing invasive pneumococcal disease, there are concerns that they may lead to serotype replacement disease; a phenomenon which has been reported in children with empyema, a complication of pneumonia. This study will assess the effectiveness of the 13-valent pneumococcal conjugate vaccine (13vPCV) program (which includesadministration of 13vPCV to children and 2, 4 and 6 months, and an 18 month booster for Aboriginal and Torres Strait Islander children residing in the NT) on hospitalised childhood pneumonia over 3 years. This study will also assess the bacterial and associated viral causes of pneumonia and empyema in children in Australia.
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Intervention code [1]
288992
0
Not applicable
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Comparator / control treatment
vaccine effectiveness will be estimated using a matched case-control analysis of PCV eligible children. For every case of SP pneumonia identified in this study, one or more date-of-birth and postcode-matched controls will be sampled from a de-identified Australian Childhood Immunisation Registry (ACIR) dataset
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Control group
Active
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Outcomes
Primary outcome [1]
291704
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Determine the real-world effectiveness of pneumococcal conjugate vaccine for preventing hospitalisation for Streptococcus pneumoniae (SP) confirmed and all-cause pneumonia; by testing patient blood, nasopharyngeal and pleural fluid samples to identify SP and perform further molecular testing to determine the isolates specific serotype. To determine vaccine effectiveness, idetified serotypes will be compared to those present in the current 13vPCV.
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Assessment method [1]
291704
0
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Timepoint [1]
291704
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At completion of the observational study (36 months)
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Secondary outcome [1]
307331
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To determine the contribution of SP to complicated and uncomplicated pneumonia in Australian children following the introduction of 13vPCV. All subjects recruited with complicated or un-complicated pneumonia will have blood and nasopharyngeal samples, +/- pleural fluid samples tested for the presence of Streptococcus pneumoniae (SP) along with other commom bacteria and viruses. SP positive samples will be further tested to identify specific PCV or non-PCV serotypes.
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Assessment method [1]
307331
0
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Timepoint [1]
307331
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At the completion of the observational study (36 months)
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Secondary outcome [2]
307501
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To assess SP serotype replacement by comparing the distribution of serotypes causing complicated and uncomplicated SP pneumonia with those obtained for complicated pneumonia before the introduction of 13vPCV.
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Assessment method [2]
307501
0
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Timepoint [2]
307501
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At the completion of the observational study (36 months)
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Secondary outcome [3]
307502
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To determine the contribution of non-SP bacterial causes of complicated childhood pneumonia.
Culture of Blood +/- pleural fluid samples will be performed at each participating site as per hospital operating procedures. Specific molecular testing will occur using in-house PCR's to detect non-SP bacteria such as Haemophilus influenzae, MSSA & MRSA
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Assessment method [3]
307502
0
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Timepoint [3]
307502
0
At the completion of the observational study (36 months)
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Secondary outcome [4]
307503
0
To determine the contribution of infection with respiratory viruses to pneumonia in children, and to assess the role of viral co-infection in pneumococcal pneumonia.
Nasopharyngeal samples from patients with complicated and un-complicated pneumonia will be cultured on enhanced growth medium to identify SP and other pathogens.
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Assessment method [4]
307503
0
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Timepoint [4]
307503
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At the completion of the observational study (36 months)
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Eligibility
Key inclusion criteria
1. Children < 18 years old hospitalized <24 hours
2. Xray confirmed pneumonia
3. Presumed infective aetiology
4. A full blood count performed and at least 250microL of blood in an EDTA tube available for further testing.
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Minimum age
0
Years
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Maximum age
18
Years
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
1. Significant co-morbidity, including haematologic malignancy, post stem cell or solid organ transplantation, cystic fibrosis, congenital malformation of the lung
2. Hospitalised within 14 days of presentation
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Study design
Purpose
Natural history
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Duration
Cross-sectional
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Selection
Case control
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Timing
Prospective
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Statistical methods / analysis
The distribution of SP serotypes among empyema cases for the 7vPCV (from ARNiE) and 13vPCV periods will be compared using two-tailed chi square statistic or Fisher’s exact test for contingency tables.
The vaccination status of cases and each of its matched controls will be referenced with regard to the date of hospitalisation of the case. The vaccination status of each case (0 doses, 1 dose, 2 doses, or 3 or more doses) will be compared with that of matched controls using conditional logistic regression analysis to estimate the odds ratio of vaccination for cases versus controls. VE will be inferred from the odds ratio (ie. VE = 1 – OR*100%) with 95% confidence intervals. VE will be estimated separately for:
1. complicated SP pneumonia (empyema),
2. uncomplicated SP PwiRIM, and
3. uncomplicated SP PwoRIM.
If the absolute difference in the point estimates of VE is <20%, the VE analyses will be pooled and reported as the primary VE measure, otherwise VE estimates will be reported separately as the primary VE measure.
Secondary VE estimates will be calculated for:
1. all pneumonia
2. PCV-type SP pneumonia, and
3. non-PCV-type SP pneumonia.
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Recruitment
Recruitment status
Recruiting
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Date of first participant enrolment
Anticipated
1/06/2014
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Actual
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
2200
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
ACT,NSW,NT,QLD,SA,TAS,WA,VIC
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Recruitment hospital [1]
2194
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Sydney Children's Hospital - Randwick
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Recruitment hospital [2]
2195
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Princess Margaret Hospital - Subiaco
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Recruitment hospital [3]
2196
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The Children's Hospital at Westmead - Westmead
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Recruitment hospital [4]
2197
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Royal Children's Hospital - Herston
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Recruitment hospital [5]
2199
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Royal Darwin Hospital - Tiwi
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Recruitment hospital [6]
2200
0
Womens and Childrens Hospital - North Adelaide
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Recruitment hospital [7]
2201
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The Royal Childrens Hospital - Parkville
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Recruitment hospital [8]
2202
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John Hunter Children's Hospital - New Lambton
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Recruitment hospital [9]
2203
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Royal Hobart Hospital - Hobart
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Recruitment hospital [10]
2204
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The Canberra Hospital - Garran
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Recruitment hospital [11]
2205
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Monash Medical Centre - Clayton campus - Clayton
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Recruitment hospital [12]
2206
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Alice Springs Hospital - Alice Springs
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Recruitment hospital [13]
8400
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Lady Cilento Children's Hospital - South Brisbane
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Recruitment postcode(s) [1]
7871
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2031 - Randwick
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Recruitment postcode(s) [2]
7872
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6008 - Subiaco
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Recruitment postcode(s) [3]
7873
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2145 - Westmead
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Recruitment postcode(s) [4]
7875
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4029 - Royal Brisbane Hospital
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Recruitment postcode(s) [5]
7876
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4101 - South Brisbane
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Recruitment postcode(s) [6]
7877
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0811 - Casuarina
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Recruitment postcode(s) [7]
7878
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5006 - North Adelaide
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Recruitment postcode(s) [8]
7879
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3052 - Parkville
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Recruitment postcode(s) [9]
7881
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2305 - New Lambton Heights
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Recruitment postcode(s) [10]
7882
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7000 - Hobart
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Recruitment postcode(s) [11]
7883
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2605 - Garran
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Recruitment postcode(s) [12]
7884
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3168 - Clayton
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Recruitment postcode(s) [13]
7885
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0870 - Alice Springs
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Funding & Sponsors
Funding source category [1]
288909
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Government body
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Name [1]
288909
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National Health Medical Research Council project grant (1064841)
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Address [1]
288909
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Level 1, 16 Marcus Clarke Street
Canberra ACT 2601
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Country [1]
288909
0
Australia
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Primary sponsor type
University
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Name
University of New South Wales
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Address
High St, Kensington NSW 2052
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Country
Australia
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Secondary sponsor category [1]
287605
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Individual
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Name [1]
287605
0
Professor Adam Jaffe
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Address [1]
287605
0
School of Women's and Children's Health
Level 3 Sydney Children's Hospital
High Street, Randwick 2031 NSW
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Country [1]
287605
0
Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
290739
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Hunter New England Local Health District
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Ethics committee address [1]
290739
0
New Lambton NSW 2305
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Ethics committee country [1]
290739
0
Australia
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Date submitted for ethics approval [1]
290739
0
30/04/2014
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Approval date [1]
290739
0
31/07/2014
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Ethics approval number [1]
290739
0
EC00130
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Ethics committee name [2]
298012
0
Mater Health Services HUman Research Ethics Committee
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Ethics committee address [2]
298012
0
Raymond Terrace South Brisbane Queensland 4101
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Ethics committee country [2]
298012
0
Australia
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Date submitted for ethics approval [2]
298012
0
17/06/2014
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Approval date [2]
298012
0
08/08/2014
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Ethics approval number [2]
298012
0
EC00332
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Ethics committee name [3]
298013
0
Monash Health Human Research Ethics Committee
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Ethics committee address [3]
298013
0
Level 2, I Block Monash Medical Centre 246 Clayton Road Clayton VIC 3168
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Ethics committee country [3]
298013
0
Australia
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Date submitted for ethics approval [3]
298013
0
08/07/2014
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Approval date [3]
298013
0
24/02/2015
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Ethics approval number [3]
298013
0
14247B
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Ethics committee name [4]
298014
0
WCHN Human Research Ethics Committee
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Ethics committee address [4]
298014
0
Level 2, Samuel Way Building 72 Kings William Road Womens and Childrens Hospital North Adelaide SA 5006
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Ethics committee country [4]
298014
0
Australia
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Date submitted for ethics approval [4]
298014
0
12/08/2014
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Approval date [4]
298014
0
01/11/2014
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Ethics approval number [4]
298014
0
HREC/14/WCHN/92
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Ethics committee name [5]
298015
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Central Austrailia Human Research Ethics Committee
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Ethics committee address [5]
298015
0
Centre for Remote Health Cnr Simpson & Skinner st PO Box 4066 Alice Springs NT 0871
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Ethics committee country [5]
298015
0
Australia
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Date submitted for ethics approval [5]
298015
0
12/06/2014
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Approval date [5]
298015
0
01/08/2014
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Ethics approval number [5]
298015
0
14-247
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Ethics committee name [6]
298016
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Human Research Ethics Committee of the Northern Territory Department of Health and Menzie School of Research
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Ethics committee address [6]
298016
0
John Matthews Building Royal Darwin Hospital Campus Rocklands Drive Casuarina NT 0810
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Ethics committee country [6]
298016
0
Australia
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Date submitted for ethics approval [6]
298016
0
20/05/2014
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Approval date [6]
298016
0
18/08/2014
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Ethics approval number [6]
298016
0
2014-2219
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Ethics committee name [7]
298017
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Princess Margaret Hospital for Children HREC
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Ethics committee address [7]
298017
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Level 1, Children's Clinical Research Facility Princess Margaret Hospital Roberts Road, Subiaco Perth WA 6840
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Ethics committee country [7]
298017
0
Australia
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Date submitted for ethics approval [7]
298017
0
14/08/2014
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Approval date [7]
298017
0
18/12/2014
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Ethics approval number [7]
298017
0
2014097EP
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Ethics committee name [8]
298018
0
ACT Human Research Ethics Committee
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Ethics committee address [8]
298018
0
Building 10, Level 6 Canberra Hospital PO Box 11 Woden ACT 2606
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Ethics committee country [8]
298018
0
Australia
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Date submitted for ethics approval [8]
298018
0
17/08/2015
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Approval date [8]
298018
0
26/11/2015
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Ethics approval number [8]
298018
0
ETH.9.15.161
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Ethics committee name [9]
298019
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Tasmanian Health and Medical Human Research Ethics Committee
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Ethics committee address [9]
298019
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Office of Research Services University of Tasmania Private Bag 1 Hobart Tasmania 7001
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Ethics committee country [9]
298019
0
Australia
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Date submitted for ethics approval [9]
298019
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10/02/2015
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Approval date [9]
298019
0
05/05/2015
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Ethics approval number [9]
298019
0
H0014697
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Summary
Brief summary
Pneumonia in children is a worldwide problem and a leading cause of morbidity and mortality. Rarely pneumonia is complicated by an ‘empyema’ where fluid collects around the lung and requires drainage with a tube. Many different types of bacteria can cause pneumonia and empyema. Streptococcus pneumoniae (SP) is one of the leading causes and has more than 90 different strains. It is unknown why some children are susceptible to pneumonia from SP; some evidence from adult patients suggests that there may be a genetic reason for susceptibility to Pneumococcal infection. Furthermore, viruses are commonly found in the upper airway of children with pneumonia and increase the risk of infection with SP. Vaccination can help prevent infection with many of the strains of pneumococcus. Australia recently introduced a vaccine which covers 13 of these strains. The main aim of this study is to look at the effectiveness of this newly introduced vaccine. The study will also look at the other bacteria and viruses that can cause pneumonia in children in Australia using sensitive molecular tests.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
46898
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Prof Adam Jaffe
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Address
46898
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Level 3 Sydney Children's Hospital
School of Women's and Children's Health
High Street, Randwick 2031 NSW
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Country
46898
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Australia
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Phone
46898
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+612 93821799
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Fax
46898
0
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Email
46898
0
[email protected]
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Contact person for public queries
Name
46899
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Roxanne Strachan
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Address
46899
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Level 0, Ainsworth Building, South West Wing
Sydney Children's Hospital
High Street Randwick 2031 NSW
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Country
46899
0
Australia
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Phone
46899
0
+61293820639
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Fax
46899
0
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Email
46899
0
[email protected]
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Contact person for scientific queries
Name
46900
0
Adam Jaffe
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Address
46900
0
Level 3 Sydney Children's Hospital
School of Women's and Children's Health
High Street, Randwick 2031 NSW
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Country
46900
0
Australia
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Phone
46900
0
+61293821799
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Fax
46900
0
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Email
46900
0
[email protected]
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No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
Type
Is Peer Reviewed?
DOI
Citations or Other Details
Attachment
Plain language summary
No
results not analysed yet
Documents added automatically
Source
Title
Year of Publication
DOI
Embase
Assessing the impact of the 13 valent pneumococcal vaccine on childhood empyema in Australia.
2021
https://dx.doi.org/10.1136/thoraxjnl-2020-216032
Embase
Real world impact of 13vPCV in preventing invasive pneumococcal pneumonia in Australian children: A national study.
2023
https://dx.doi.org/10.1016/j.vaccine.2022.11.006
N.B. These documents automatically identified may not have been verified by the study sponsor.
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