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Trial registered on ANZCTR
Registration number
ACTRN12616000124437p
Ethics application status
Submitted, not yet approved
Date submitted
3/12/2015
Date registered
3/02/2016
Date last updated
3/02/2016
Type of registration
Prospectively registered
Titles & IDs
Public title
Comparison of boosting of mucosal immunity after full and fractional dose of inactivated poliovirus vaccine, clinical trial in children in Sri Lanka, 2016
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Scientific title
Comparison of boosting of mucosal immunity after full and fractional dose of inactivated poliovirus vaccine, a randomized clinical trial in 300 children aged 10-12 years of age living in Kalutara district of Sri Lanka, 2016
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Secondary ID [1]
288059
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nil
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Universal Trial Number (UTN)
U1111-1177-2137
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
poliomyelitis
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Condition category
Condition code
Infection
297169
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0
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Other infectious diseases
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Full one dose (0.5 ml) of inactivated poliovirus vaccine administered intramuscularly
or
Fractional one dose (0.1 ml) of inactivated poliovirus vaccine administered intradermally
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Intervention code [1]
293380
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Prevention
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Comparator / control treatment
no vaccine administered in the control group
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Control group
Active
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Outcomes
Primary outcome [1]
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Difference in proportion of children excreting vaccine polioviruses (by serotype) between arms among those who serologically respond to IPV measured by isolation of poliovirus in stool
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Assessment method [1]
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Timepoint [1]
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7 days after administration of live oral poliovirus vaccine
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Secondary outcome [1]
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Difference in duration of poliovirus excretion between arms measured by isolation of poliovirus in stool
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Assessment method [1]
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Timepoint [1]
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42 days after challenge with oral poliovirus vaccine
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Eligibility
Key inclusion criteria
Any child 10-12 years of age residing in the determined area of Kalutara
Parent/Guardian provides consent for child’s participation, including vaccination with IPV/OPV and blood and stool sample collections
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Minimum age
10
Years
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Maximum age
12
Years
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Sex
Both males and females
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Can healthy volunteers participate?
Yes
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Key exclusion criteria
Contraindication for venepuncture
Sick child requiring hospitalization for acute or chronic condition
Diagnosis or suspicion of congenital immunodeficiency disorder in the subject or an immediate family member
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Study design
Purpose of the study
Prevention
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
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Who is / are masked / blinded?
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Intervention assignment
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Other design features
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Phase
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Type of endpoint/s
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Statistical methods / analysis
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Recruitment
Recruitment status
Not yet recruiting
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Date of first participant enrolment
Anticipated
15/02/2016
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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
300
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Accrual to date
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Final
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Recruitment outside Australia
Country [1]
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Sri Lanka
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State/province [1]
7392
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Funding & Sponsors
Funding source category [1]
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Other
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Name [1]
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World Health Organisation
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Address [1]
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Avenue Appia 20
CH-1211 Geneva 27 Suisse
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Country [1]
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Switzerland
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Primary sponsor type
Other
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Name
World Health Organization
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Address
Avenue Appia 20
CH-1211 Geneva 27 Switzerland
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Country
Switzerland
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Secondary sponsor category [1]
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None
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Name [1]
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none
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Address [1]
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none
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Country [1]
291207
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Ethics approval
Ethics application status
Submitted, not yet approved
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Ethics committee name [1]
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World Health Organisation
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Ethics committee address [1]
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Avenue Appia 20 CH-1211 Geneva 27 Suisse
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Ethics committee country [1]
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Switzerland
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Date submitted for ethics approval [1]
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01/12/2015
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Approval date [1]
293964
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Ethics approval number [1]
293964
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Summary
Brief summary
This study will evaluate the effect of fIPV on boosting mucosal immunity against polioviruses in Sri Lanka, a country with high routine immunization coverage with OPV and IPV introduced in its routine immunization schedule. It will enable decision makers in Sri Lanka as well as in other countries in similar situation, to evaluate risks and benefits of fIPV use for OBR in case of cVDPV2 outbreak following the tOPV to bOPV switch. After April 2016, no country will be allowed to use tOPV therefore this is a last chance to conduct this type of a study and all study procedures must be completed by the end of April 2016.
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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
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Dr Paba Palihawadana
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Address
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Epidemiology Unit , Ministry of Health,Sri Lanka.
231, De Saram Road, Colombo 10
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Country
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Sri Lanka
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Phone
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+94-112 695 112
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Fax
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Email
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[email protected]
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Contact person for public queries
Name
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Ondrej Mach
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Address
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World Health Organization
Avenue Appia 20
CH-1211 Geneva 27 Suisse
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Country
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Switzerland
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Phone
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+41227911863
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Fax
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Email
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[email protected]
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Contact person for scientific queries
Name
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ondrej mach
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Address
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World Health Organization
Avenue Appia 20
CH-1211 Geneva 27 Suisse
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Country
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Switzerland
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Phone
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+41227911863
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Fax
61960
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Email
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[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
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
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