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Effectiveness Assessment of Vaccinating Schoolchildren Against Influenza (Xo_Gripe)

Primary Purpose

Influenza, Acute Respiratory Infection

Status
Completed
Phase
Phase 4
Locations
Brazil
Study Type
Interventional
Intervention
Influenza vaccine
Control vaccine
Sponsored by
Butantan Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Influenza focused on measuring Influenza, Vaccination, Vaccines, Schoolchildren, Effectiveness, Intervention studies, Adolescents, Laboratory Confirmed Influenza

Eligibility Criteria

6 Years - 18 Years (Child, Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • older than six years of age;
  • live in the study area;
  • parent consent to participate, by signing the Informed Consent Form;
  • no history of anaphilaxis or hipersensitivity to eggs or eggs proteins;
  • no history no history anaphilaxis or hipersensitivity to any substances;
  • no acute disease at the moment of vaccination
  • no use of immunesupressant drugs;
  • not have received any other vaccine in the previous six months;
  • no participation in other clinical trial in the previous six months.

Exclusion Criteria:

  • Any condition above mentioned.

Sites / Locations

  • Butantan Institute

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Sham Comparator

Arm Label

Influenza vaccine

Control vaccine

Arm Description

Schoolchildren from 6 to 8 years received two intra-muscular doses of 0.5 ml of inactivated influenza vaccine, of the Southern Hemisphere, 2009. Schoolchildren above 8 years received one intra-muscular dose of 0.5 ml of inactivated influenza vaccine, of the Southern Hemisphere, 2009.

Schoolchildren received one intra-muscular dose of 0.5 ml of Meningococcal C conjugate vaccine. Schoolchildren under nine years of age received also one intra-muscular dose of 0.5 ml of varicella vaccine one month after the Meningococcal C vaccine.

Outcomes

Primary Outcome Measures

Laboratory confirmed influenza
RT-PCR confirmed influenza in respiratory secretions samples

Secondary Outcome Measures

Acute Repiratory Infection (ARI)
Presence of at least of two symptoms of ARI: fever, cough, sore throat, headache, appetite loss, running nose

Full Information

First Posted
September 10, 2012
Last Updated
April 3, 2023
Sponsor
Butantan Institute
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1. Study Identification

Unique Protocol Identification Number
NCT01693380
Brief Title
Effectiveness Assessment of Vaccinating Schoolchildren Against Influenza
Acronym
Xo_Gripe
Official Title
Effectiveness Assessment of Vaccinating Schoolchildren Against Influenza the in São Paulo, 2009
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Completed
Study Start Date
May 2009 (Actual)
Primary Completion Date
June 2009 (Actual)
Study Completion Date
November 2009 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Butantan Institute

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Vaccinating schoolchildren against influenza would prevent the disease among non-vaccinated household members.
Detailed Description
Children and adolescents play an important role in sustaining the transmission of influenza. Moreover, with the occurrence of influenza in children, there are important socioeconomic consequences to families affected by the disease, related to absenteeism, expenditure on health services and medication use. This study presents an evaluation of direct and indirect effectiveness of influenza vaccination in school age children and their unvaccinated household contacts. It was conducted in 2009, in Sao Paulo - Brazil, through a randomized double-blind community trial, with six months of follow up. For the evaluation of vaccine effectiveness, the influenza vaccine was used for the experimental group, and meningitis conjugate and varicella vaccines for the control group. After vaccination, the volunteers and their families were followed for six months, in order to identify cases of acute respiratory infection (ARI) and to collect biological samples for testing with RT-PCR for diagnosis of influenza.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Influenza, Acute Respiratory Infection
Keywords
Influenza, Vaccination, Vaccines, Schoolchildren, Effectiveness, Intervention studies, Adolescents, Laboratory Confirmed Influenza

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
1742 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Influenza vaccine
Arm Type
Experimental
Arm Description
Schoolchildren from 6 to 8 years received two intra-muscular doses of 0.5 ml of inactivated influenza vaccine, of the Southern Hemisphere, 2009. Schoolchildren above 8 years received one intra-muscular dose of 0.5 ml of inactivated influenza vaccine, of the Southern Hemisphere, 2009.
Arm Title
Control vaccine
Arm Type
Sham Comparator
Arm Description
Schoolchildren received one intra-muscular dose of 0.5 ml of Meningococcal C conjugate vaccine. Schoolchildren under nine years of age received also one intra-muscular dose of 0.5 ml of varicella vaccine one month after the Meningococcal C vaccine.
Intervention Type
Biological
Intervention Name(s)
Influenza vaccine
Intervention Description
Influenza vaccine: schoolchidren in the experimental group received IM administered: From 6 to 9 years of age - 2 doses (0.5ml each) of the tri-valent innactivated influenza vaccine - Southern Hemisphere formulation, 2009 - one month apart. 9 years of age and older: one dose (0.5ml) of the tri-valent innactivated influenza vaccine - Southern Hemisphere formulation, 2009 - one month apart.
Intervention Type
Biological
Intervention Name(s)
Control vaccine
Other Intervention Name(s)
Meningococcal C conjugate vaccine, Varicella vaccine
Intervention Description
Schoolchildren from 6 to 8 years of age: - One dose (0.5ml), IM administered, of Meningococcal C conjugate vaccine, and one dose (0.5ml), one month later, of varicella vaccine, IM administered.
Primary Outcome Measure Information:
Title
Laboratory confirmed influenza
Description
RT-PCR confirmed influenza in respiratory secretions samples
Time Frame
June 01, 2009 to November 30, 2009
Secondary Outcome Measure Information:
Title
Acute Repiratory Infection (ARI)
Description
Presence of at least of two symptoms of ARI: fever, cough, sore throat, headache, appetite loss, running nose
Time Frame
6 months
Other Pre-specified Outcome Measures:
Title
Number of participantes with any adverse event as a measure of safety and tolerability
Description
Any solicited or unsolicited adverse event
Time Frame
30 days after vaccination

10. Eligibility

Sex
All
Minimum Age & Unit of Time
6 Years
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: older than six years of age; live in the study area; parent consent to participate, by signing the Informed Consent Form; no history of anaphilaxis or hipersensitivity to eggs or eggs proteins; no history no history anaphilaxis or hipersensitivity to any substances; no acute disease at the moment of vaccination no use of immunesupressant drugs; not have received any other vaccine in the previous six months; no participation in other clinical trial in the previous six months. Exclusion Criteria: Any condition above mentioned.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Expedito J Luna, MD
Organizational Affiliation
University of Sao Paulo
Official's Role
Principal Investigator
Facility Information:
Facility Name
Butantan Institute
City
Sao Paulo
ZIP/Postal Code
05503900
Country
Brazil

12. IPD Sharing Statement

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Effectiveness Assessment of Vaccinating Schoolchildren Against Influenza

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