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Influenza Immunization of Children in India

Primary Purpose

Influenza

Status
Completed
Phase
Phase 4
Locations
India
Study Type
Interventional
Intervention
Inactivated Trivalent Influenza Vaccine (TIV)
Inactivated poliovirus vaccine (IPV), trivalent
Sponsored by
University of Colorado, Denver
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Influenza focused on measuring Influenza, India, Children, Trivalent Influenza Vaccine (TIV), Inactivated poliovirus vaccine (IPV), Direct influenza vaccine effectiveness, Total influenza vaccine effectiveness, Indirect influenza vaccine effectiveness

Eligibility Criteria

6 Months - 10 Years (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

Inclusion in either vaccine group (TIV or IPV) will require ages 6 months through 10 years of age.

All individuals in enrolled households will be eligible for enrollment into surveillance arm.

Exclusion Criteria:

Exclusion criteria from the vaccine groups includes known allergy to eggs, or hypersensitivity to other components of the vaccines.

Sites / Locations

  • Comprehensive Rural Health Services Project

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Placebo Comparator

No Intervention

Arm Label

Inactivated Trivalent Influenza Vaccine

Inactivated Polio Vaccine

Surveillance arm

Arm Description

Inactivated trivalent influenza vaccine (TIV), split virion

Inactivated poliovirus vaccine (IPV), trivalent

Those ineligible for vaccination will be enrolled for febrile acute respiratory illness (FARI) surveillance to assess indirect effects of vaccination in household members.

Outcomes

Primary Outcome Measures

Laboratory-confirmed influenza infection in vaccinated child

Secondary Outcome Measures

Laboratory-confirmed influenza infection in household member of a vaccinated child.

Full Information

First Posted
September 4, 2012
Last Updated
March 23, 2017
Sponsor
University of Colorado, Denver
Collaborators
All India Institute of Medical Sciences, New Delhi, International Clinical Epidemiology Network (INCLEN) TRUST, University of Alabama at Birmingham, Centers for Disease Control and Prevention
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1. Study Identification

Unique Protocol Identification Number
NCT01680679
Brief Title
Influenza Immunization of Children in India
Official Title
Influenza Immunization of Children in India
Study Type
Interventional

2. Study Status

Record Verification Date
March 2017
Overall Recruitment Status
Completed
Study Start Date
May 2012 (undefined)
Primary Completion Date
May 2014 (Actual)
Study Completion Date
May 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Colorado, Denver
Collaborators
All India Institute of Medical Sciences, New Delhi, International Clinical Epidemiology Network (INCLEN) TRUST, University of Alabama at Birmingham, Centers for Disease Control and Prevention

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Influenza viruses are significant causes of human illness and death in developed and developing countries. This study will measure the ability of influenza vaccine given to children in India to protect both the children and unimmunized persons around them from influenza. It will also determine whether the best time to immunize in a country like India that has both summer and winter outbreaks of influenza is in the fall, as is done now, or whether immunization should be in the spring to protect against influenza infections in the summer.
Detailed Description
Although influenza vaccines are used routinely in the United States, including in young children, influenza vaccines have not seen widespread use in India. This is likely contributed to by the lack of information from India about disease burden due to influenza and because influenza vaccines have not been tested for efficacy in India. In addition, because young children are thought to be important in the spread of influenza in families, it is possible immunization of children against influenza will reduce influenza infections among older children and adults in the home. The study described here is an extension of an earlier study (ClinicalTrials.gov NCT00934245) that tested the use of immunization against influenza in the fall. The current study will administer influenza vaccine in the spring prior to the summer monsoon rains that are associated with peaks of influenza activity in parts of India. Reduction of influenza infections among the influenza immunized children and their household members will be compared to the children and household members in the control vaccine group.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Influenza
Keywords
Influenza, India, Children, Trivalent Influenza Vaccine (TIV), Inactivated poliovirus vaccine (IPV), Direct influenza vaccine effectiveness, Total influenza vaccine effectiveness, Indirect influenza vaccine effectiveness

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
18163 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Inactivated Trivalent Influenza Vaccine
Arm Type
Experimental
Arm Description
Inactivated trivalent influenza vaccine (TIV), split virion
Arm Title
Inactivated Polio Vaccine
Arm Type
Placebo Comparator
Arm Description
Inactivated poliovirus vaccine (IPV), trivalent
Arm Title
Surveillance arm
Arm Type
No Intervention
Arm Description
Those ineligible for vaccination will be enrolled for febrile acute respiratory illness (FARI) surveillance to assess indirect effects of vaccination in household members.
Intervention Type
Biological
Intervention Name(s)
Inactivated Trivalent Influenza Vaccine (TIV)
Intervention Type
Biological
Intervention Name(s)
Inactivated poliovirus vaccine (IPV), trivalent
Primary Outcome Measure Information:
Title
Laboratory-confirmed influenza infection in vaccinated child
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Laboratory-confirmed influenza infection in household member of a vaccinated child.
Time Frame
1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
6 Months
Maximum Age & Unit of Time
10 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Inclusion in either vaccine group (TIV or IPV) will require ages 6 months through 10 years of age. All individuals in enrolled households will be eligible for enrollment into surveillance arm. Exclusion Criteria: Exclusion criteria from the vaccine groups includes known allergy to eggs, or hypersensitivity to other components of the vaccines.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Wayne Sullender, MD
Organizational Affiliation
University of Colorado, Denver
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Shobha Broor, MD
Organizational Affiliation
All India Institute of Medical Sciences, New Delhi
Official's Role
Principal Investigator
Facility Information:
Facility Name
Comprehensive Rural Health Services Project
City
Ballabgarh
State/Province
Haryana
Country
India

12. IPD Sharing Statement

Learn more about this trial

Influenza Immunization of Children in India

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