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Acetaminophen Before Vaccines for Infants Study (AVIS)

Primary Purpose

Fever

Status
Completed
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Acetaminophen
placebo
Sponsored by
Kaiser Permanente
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Fever focused on measuring Acetaminophen, Vaccination, Immunization

Eligibility Criteria

6 Weeks - 9 Months (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria: Child is a current Group Health enrollee. Child will be seen at a Group Health clinic for a Well Child visit that is expected to include 2 or more vaccines after 6 wks and before 10 months of age. Exclusion Criteria: If child was born at less than 36 weeks of gestation, the child is not eligible until 4 months of age or older. If the child's birth weight was less than 5.5 pounds (2500 grams), the child is not eligible until 4 months of age or older.

Sites / Locations

  • Group Health Research Institute

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Acetaminophen

Placebo

Arm Description

Children were randomized 1:1 to receive up to five doses of acetaminophen (10-15mg per kg) or placebo following routine vaccinations.

Children were randomized 1:1 to receive up to five doses of acetaminophen (10-15mg per kg) or placebo following routine vaccinations.

Outcomes

Primary Outcome Measures

Fever >=38C Within 32 Hours of Vaccination.
Fever, defined as rectal temperature >=38C within 32 hours of vaccination.

Secondary Outcome Measures

Fever >=39C Within 32 Hours of Vaccination.
Fever, defined as rectal temperature >=39C within 32 hours of vaccination.
Study Assignment Unblinded
The need for unblinding at any time during the study
Medical Utilization
Telephone calls to the consulting nurse or the child's physician that were made due to concerns regarding an acute illness, fever, or possible vaccine reaction and outpatient, urgent care, and emergency room visits that were for evaluation of an acute illness, fever, or a possible vaccine reaction, within 32 hours of vaccination.
Infant Fussiness
Parents were asked to record level of fussiness (compared with the child's usual) within 32 hours of vaccination, using the categories much less than usual, less than usual, about usual, more than usual, and much more than usual.
Parent Time Lost From Sleep
Parents were asked about their sleep on the night following the vaccinations. They were asked to report whether they slept much less than usual, less than usual, about the usual amount, more than usual, or much more than usual on that night.
Infant Time Lost From Sleep
Parents were asked about their infant's sleep on the night following the vaccinations. They were asked to report whether their infant slept much less than usual, less than usual, about the usual amount, more than usual, or much more than usual on that night.
Parent Time Lost From Work
Parents were asked to report whether they were scheduled to work on the day of the vaccination visit (but following that visit) or the next day and, if so, whether they had to miss work to care for their infant because of fever, fussiness, or possible vaccine reaction on those days.

Full Information

First Posted
May 11, 2006
Last Updated
October 11, 2017
Sponsor
Kaiser Permanente
Collaborators
Centers for Disease Control and Prevention
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1. Study Identification

Unique Protocol Identification Number
NCT00325819
Brief Title
Acetaminophen Before Vaccines for Infants Study (AVIS)
Official Title
A Randomized Placebo-controlled Trial of Acetaminophen for Prevention of Post-vaccination Fever in Infants
Study Type
Interventional

2. Study Status

Record Verification Date
October 2017
Overall Recruitment Status
Completed
Study Start Date
May 2006 (undefined)
Primary Completion Date
September 2009 (Actual)
Study Completion Date
September 2009 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Kaiser Permanente
Collaborators
Centers for Disease Control and Prevention

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to see whether giving acetaminophen (the medicine in Tylenol) for routine infant vaccinations is helpful in preventing fever or other symptoms.
Detailed Description
Post-vaccination fever occurs in up to 40% of infants receiving routinely recommended childhood vaccinations. Although serious events are rare, post-vaccination fever causes discomfort for the child, can lead to medical utilization, can rarely result in febrile seizure, and can cause a working parent to miss time from their job to care for a febrile infant who cannot attend day care. The benefits of acetaminophen prophylaxis for infants receiving current vaccinations, in terms of reduction of discomfort for the child, improvement of quality-of-life indicators for the parent, or reduction of medical utilization, have not been measured. This randomized, blinded, placebo-controlled trial will assess the efficacy of prophylaxis with acetaminophen in prevention of fever following routine childhood immunizations.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fever
Keywords
Acetaminophen, Vaccination, Immunization

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
374 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Acetaminophen
Arm Type
Active Comparator
Arm Description
Children were randomized 1:1 to receive up to five doses of acetaminophen (10-15mg per kg) or placebo following routine vaccinations.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Children were randomized 1:1 to receive up to five doses of acetaminophen (10-15mg per kg) or placebo following routine vaccinations.
Intervention Type
Drug
Intervention Name(s)
Acetaminophen
Intervention Description
Children were randomized 1:1 to receive up to five doses of acetaminophen (10-15mg per kg) or placebo following routine vaccinations.
Intervention Type
Other
Intervention Name(s)
placebo
Intervention Description
Children were randomized 1:1 to receive up to five doses of acetaminophen (10-15mg per kg) or placebo following routine vaccinations.
Primary Outcome Measure Information:
Title
Fever >=38C Within 32 Hours of Vaccination.
Description
Fever, defined as rectal temperature >=38C within 32 hours of vaccination.
Time Frame
Fever within 32 hours following vaccination
Secondary Outcome Measure Information:
Title
Fever >=39C Within 32 Hours of Vaccination.
Description
Fever, defined as rectal temperature >=39C within 32 hours of vaccination.
Time Frame
Fever within 32 hours following vaccination
Title
Study Assignment Unblinded
Description
The need for unblinding at any time during the study
Time Frame
At any time during participation in the study
Title
Medical Utilization
Description
Telephone calls to the consulting nurse or the child's physician that were made due to concerns regarding an acute illness, fever, or possible vaccine reaction and outpatient, urgent care, and emergency room visits that were for evaluation of an acute illness, fever, or a possible vaccine reaction, within 32 hours of vaccination.
Time Frame
Within 32 hours of vaccination.
Title
Infant Fussiness
Description
Parents were asked to record level of fussiness (compared with the child's usual) within 32 hours of vaccination, using the categories much less than usual, less than usual, about usual, more than usual, and much more than usual.
Time Frame
Within 32 hours of vaccination
Title
Parent Time Lost From Sleep
Description
Parents were asked about their sleep on the night following the vaccinations. They were asked to report whether they slept much less than usual, less than usual, about the usual amount, more than usual, or much more than usual on that night.
Time Frame
On the night following vaccinations
Title
Infant Time Lost From Sleep
Description
Parents were asked about their infant's sleep on the night following the vaccinations. They were asked to report whether their infant slept much less than usual, less than usual, about the usual amount, more than usual, or much more than usual on that night.
Time Frame
On the night following vaccinations
Title
Parent Time Lost From Work
Description
Parents were asked to report whether they were scheduled to work on the day of the vaccination visit (but following that visit) or the next day and, if so, whether they had to miss work to care for their infant because of fever, fussiness, or possible vaccine reaction on those days.
Time Frame
Through the day after vaccination

10. Eligibility

Sex
All
Minimum Age & Unit of Time
6 Weeks
Maximum Age & Unit of Time
9 Months
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Child is a current Group Health enrollee. Child will be seen at a Group Health clinic for a Well Child visit that is expected to include 2 or more vaccines after 6 wks and before 10 months of age. Exclusion Criteria: If child was born at less than 36 weeks of gestation, the child is not eligible until 4 months of age or older. If the child's birth weight was less than 5.5 pounds (2500 grams), the child is not eligible until 4 months of age or older.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lisa A Jackson, MD, MPH
Organizational Affiliation
Kaiser Permanente
Official's Role
Principal Investigator
Facility Information:
Facility Name
Group Health Research Institute
City
Seattle
State/Province
Washington
ZIP/Postal Code
98101
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
21698100
Citation
Jackson LA, Peterson D, Dunn J, Hambidge SJ, Dunstan M, Starkovich P, Yu O, Benoit J, Dominguez-Islas CP, Carste B, Benson P, Nelson JC. A randomized placebo-controlled trial of acetaminophen for prevention of post-vaccination fever in infants. PLoS One. 2011;6(6):e20102. doi: 10.1371/journal.pone.0020102. Epub 2011 Jun 17.
Results Reference
result

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Acetaminophen Before Vaccines for Infants Study (AVIS)

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