- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01432340
Seasonal Influenza Vaccine Effectiveness Study in Kenya
Seasonal Influenza Vaccine Effectiveness Study in the Kenyan Communities of Kibera and Lwak
Study Overview
Status
Intervention / Treatment
Detailed Description
Vaccine will be donated by Sanofi Pasteur in a quantity large enough to vaccinate the eligible population. Vaccine will be made available to infants from 6 months of age through children up to 10 years old. This includes an age group that is at high risk for severe outcomes (<5 years) and an age group (school-age children, 5-10) that is considered most likely to spread the infection.
Ascertainment of Influenza Illness:
Primary Outcome Measure
• Laboratory-confirmed influenza infection
Secondary outcome measures
- Medically attended ILI, SARI
- Community-reported ILI SARI
- Laboratory-confirmed influenza, medically attended ILI and SARI, and community-reported ILI and SARI in non-immunized household members
In Lwak and Kibera, field workers visit households weekly and encourage residents to go to the free clinic if they have respiratory symptoms. Currently, from KEMRI/CDC surveillance data, in Kibera, approximately 57 % of people in the catchment area seek medical care for ILI (Range: 62% children - 52% adults) and of those people who seek care, 72% seek care at Tabitha clinic. In Lwak, approximately 77% of people in the catchment area seek medical care for ILI (Range: 75% children - 80% adults) and of those people who seek care, 34% seek care at Lwak clinic.
The surveillance for ILI and SARI will continue as usual, with weekly field worker (also called community interviewer) household visits, clinic-based surveillance for ILI and SARI at Tabitha clinic and Lwak clinic, and sampling of all patients who meet the case definition for ILI and SARI
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
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Nairobi, Kenya
- KEMRI/CDC IEIP surveillance- Kibera
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Western
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Kisumu, Western, Kenya
- KEMRI/CDC- IEIP surveillance-Asembo
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Age 6months -10 years
- Enrolled in the IEIP morbidity study
Exclusion Criteria:
- Age less than 6 months or greater than or equal to 11 years
- Not enrolled in the IEIP morbidity study
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Vaccinated group
Children between 6months- 10years of age who have received the influenza vaccine
|
annual recommended Southern Hemisphere vaccine
Other Names:
|
|
Unvaccinated group
Eligible children between 6months and 10years who didn't receive the influenza vaccine
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annual recommended Southern Hemisphere vaccine
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Laboratory-confirmed influenza infection
Time Frame: June 2010-March 2013 (3 yrs)
|
Look at the number of vaccinated children who develop laboratory-confirmed influenza infection compared to a matched unvaccinated group of children.
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June 2010-March 2013 (3 yrs)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Medically attended Influenza Like Illness(ILI) and Severe Acute Respiratory Illness (SARI)
Time Frame: June 2011-March 2013 (2 yrs)
|
Look at the number of medically attended ILI and SARI in the unvaccinated group and compare to the vaccinated goup
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June 2011-March 2013 (2 yrs)
|
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Community-reported ILI SARI
Time Frame: June 2011- March 2013 (2 yrs)
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Look at the number of Community-reported ILI and SARI in the unvaccinated group and compare to the number in the vaccinated group
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June 2011- March 2013 (2 yrs)
|
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Laboratory-confirmed influenza, medically attended ILI and SARI, and community-reported ILI and SARI in non-immunized household members
Time Frame: June 2011-March 2013 (2 yrs)
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Look at the number of Laboratory-confirmed influenza, medically attended ILI and SARI, and community-reported ILI and SARI in non-immunized household members in both households that have a vaccinated child versus households that didn't have a vaccinated child
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June 2011-March 2013 (2 yrs)
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Mark A Katz, MD, Center for Disease Control and Prevention-Kenya
- Principal Investigator: Robert Breiman, MD, Centers for Disease Control and Prevention
- Principal Investigator: Joshua Mott, PhD, Centers for Disease Control and Prevention
Publications and helpful links
General Publications
- World Health Organization. Acute Respiratory Infections (Update September 2009). 2009. Available at http://www.who.int/vaccine_research/diseases/ari/en/print.html
- Williams BG, Gouws E, Boschi-Pinto C, Bryce J, Dye C. Estimates of world-wide distribution of child deaths from acute respiratory infections. Lancet Infect Dis. 2002 Jan;2(1):25-32. doi: 10.1016/s1473-3099(01)00170-0.
- Viboud C, Alonso WJ, Simonsen L. Influenza in tropical regions. PLoS Med. 2006 Apr;3(4):e89. doi: 10.1371/journal.pmed.0030089. Epub 2006 Mar 7.
- Belongia EA, Kieke BA, Donahue JG, Greenlee RT, Balish A, Foust A, Lindstrom S, Shay DK; Marshfield Influenza Study Group. Effectiveness of inactivated influenza vaccines varied substantially with antigenic match from the 2004-2005 season to the 2006-2007 season. J Infect Dis. 2009 Jan 15;199(2):159-67. doi: 10.1086/595861.
- Center for Disease Control. ACIP Provisional Recommendations for the Use of Influenza Vaccines, March 2, 2010. Available at http://www.immunize.org/acip/
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- CDC-NCIRD-5933
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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