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Acetaminophen Versus Ibuprofen in Children With Asthma (AVICA)

Primary Purpose

Asthma, Wheezing

Status
Completed
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Acetaminophen
Ibuprofen
Sponsored by
Milton S. Hershey Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Asthma focused on measuring Asthma, Wheezing, Ibuprofen, Acetaminophen, exacerbations, pain, fever

Eligibility Criteria

12 Months - 59 Months (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 12-59 months of age.
  • If the child is not currently taking long-term asthma controller therapy (meaning that the child has taken no inhaled corticosteroid or leukotriene receptor antagonist medication whatsoever over the past 6 months), then one of the following criteria must be met:

    • Daytime asthma symptoms more than two days per week (average over the past 4 weeks),
    • At least one nighttime awakening from asthma (over the past 4 weeks),
    • Two or more asthma exacerbations requiring systemic corticosteroids in the previous 6 months,
    • Four or more wheezing episodes in the previous 12 months.
  • If the child is currently taking long-term asthma controller therapy (meaning that the child has taken daily or intermittent/as-needed inhaled corticosteroid or leukotriene receptor antagonist over the past 6 months), then one of the following criteria must be met:

    • Taking inhaled corticosteroid or leukotriene receptor antagonist for more than 3 months (or more than 90 days) out of the previous 6 months (or 180 days),
    • Daytime asthma symptoms more than two days per week (average over the past 4 weeks),
    • More than one nighttime awakening from asthma (over the past 4 weeks),
    • Two or more asthma exacerbations requiring systemic corticosteroids in the previous 12 months,
    • Four or more wheezing episodes in the previous 12 months.
  • Up to date with immunizations, including varicella (unless the subject has already had clinical varicella).
  • Willingness to provide informed consent by the child's parent or guardian.

Exclusion Criteria:

  • Allergic reaction to the study medications or any component of the study drugs, including (but not limited to) urticaria, rash, angioedema, or hypotension following delivery,
  • Chronic medical disorders that could interfere with drug metabolism/excretion (for instance chronic hepatic, biliary, or renal disease),
  • Chronic medical disorders that may increase the risk of drug-related injury, including (but not limited to):

    • Osteogenesis imperfecta (increased risk of bone demineralization/fracture with corticosteroid therapy),
    • Crohn's disease, ulcerative colitis, juvenile rheumatoid arthritis, clotting disorders, or Factor deficiency (increased risk of bleeding with corticosteroid therapy),
    • G6PD deficiency (increased risk of hemolytic anemia with acetaminophen use),
    • Phenylketonuria (potential for aspartame exposure with study interventions),
    • Seizure disorder treated with anticonvulsants (risk of acetaminophen toxicity with carbamazepine), or
    • History of clotting disorders or Factor deficiency (increased risk of bleeding with corticosteroids),
  • Co-morbid disorders associated with wheezing including (but not limited to) immune deficiency disorders, cystic fibrosis, aspiration, clinically-relevant gastroesophageal reflux, tracheomalacia, congenital airway anomalies (clefts, fistulas, slings, rings), bronchiectasis, bronchopulmonary dysplasia, and/or history of premature birth before 35 weeks gestation,
  • Significant developmental delay/failure to thrive, defined as 5th percentile for height and/or weight or crossing of two major percentile lines during the last year for age and sex,
  • History of a near-fatal asthma exacerbation requiring intubation or assisted ventilation,
  • No primary medical caregiver (e.g., a nurse practitioner, physician assistant, physician, or group medical practice such as a hospital-based clinic) whom the subject can contact for primary medical care,
  • Three or more hospitalizations in the previous 12 months for wheezing or respiratory illnesses,
  • Treatment with 5 or more courses of systemic corticosteroids (oral, intramuscular or intravenous) in the past 6 months,
  • Current use of higher than step 2 NAEPP asthma guideline therapy
  • If receiving allergy shots, change in the dose within the past 3 months.

Sites / Locations

  • University of Arizona College of Medicine
  • Children's Hospital & Research Center Oakland
  • UCSF Benioff Children's Hospital
  • National Jewish Health
  • Emory University
  • Rush University Medical Center/Stroger Hospital
  • Children's Memorial Hospital
  • Children's Hospital Boston
  • Children's Hospital, Boston
  • St. Louis Children's Hospital
  • Wake Forest University Health Sciences
  • Rainbow Babies and Children's Hospital, Case Western Reserve University
  • Children's Hospital of Pittsburgh of UPMC
  • University of Virginia Health System
  • University of Wisconsin-Madison

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

acetaminophen

ibuprofen

Arm Description

acetaminophen given as needed for pain or fever

ibuprofen given as needed for pain or fever

Outcomes

Primary Outcome Measures

Exacerbation Frequency
the number of asthma exacerbations requiring systemic corticosteroids

Secondary Outcome Measures

Asthma Control Days
proportion of study days on which asthma was controlled, measured by electronic diary
Asthma Rescue Medication Use
average albuterol rescue use per week, measured by electronic diary
Health Care Utilization
frequency of unscheduled physician visits, emergency department visits or hospitalizations for asthma

Full Information

First Posted
May 23, 2012
Last Updated
November 17, 2016
Sponsor
Milton S. Hershey Medical Center
Collaborators
National Heart, Lung, and Blood Institute (NHLBI)
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1. Study Identification

Unique Protocol Identification Number
NCT01606319
Brief Title
Acetaminophen Versus Ibuprofen in Children With Asthma
Acronym
AVICA
Official Title
Acetaminophen vs. Ibuprofen in Children With Asthma
Study Type
Interventional

2. Study Status

Record Verification Date
November 2016
Overall Recruitment Status
Completed
Study Start Date
February 2013 (undefined)
Primary Completion Date
April 2015 (Actual)
Study Completion Date
April 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Milton S. Hershey Medical Center
Collaborators
National Heart, Lung, and Blood Institute (NHLBI)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The Acetaminophen Versus Ibuprofen in Children with Asthma study will test the primary hypothesis that in preschool children 12-59 months of age with persistent asthma on standardized asthma therapy, the number of asthma exacerbations requiring systemic corticosteroids will be more frequent in children randomized to receive acetaminophen as compared to those randomized to receive ibuprofen on an as needed basis for fevers and pain.
Detailed Description
AVICA is a 48-week randomized therapeutic trial involving two parallel treatment arms: acetaminophen and ibuprofen. Participating children will be randomized to receive either acetaminophen or ibuprofen administered as needed per parental decision for fever and analgesia. This study will address which is the most appropriate antipyretic-analgesic medication in young children with asthma, and will inform both clinicians and parents seeking to treat children with fever and pain. Given the high frequency of administration of these drugs, this study will have a significant impact on pediatric healthcare regardless of whether a differential effect is discovered as significant uncertainty currently exists as to whether acetaminophen use is associated with increased asthma symptoms.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Asthma, Wheezing
Keywords
Asthma, Wheezing, Ibuprofen, Acetaminophen, exacerbations, pain, fever

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
300 (Actual)

8. Arms, Groups, and Interventions

Arm Title
acetaminophen
Arm Type
Experimental
Arm Description
acetaminophen given as needed for pain or fever
Arm Title
ibuprofen
Arm Type
Experimental
Arm Description
ibuprofen given as needed for pain or fever
Intervention Type
Drug
Intervention Name(s)
Acetaminophen
Other Intervention Name(s)
tylenol, paracetamol
Intervention Description
15 mg/kg every 6 hours as needed
Intervention Type
Drug
Intervention Name(s)
Ibuprofen
Other Intervention Name(s)
motrin, advil, nonsteroidal anti-inflammatory drug
Intervention Description
9.4 mg/kg every 6 hours as needed
Primary Outcome Measure Information:
Title
Exacerbation Frequency
Description
the number of asthma exacerbations requiring systemic corticosteroids
Time Frame
last 46 weeks of 48 week treatment period
Secondary Outcome Measure Information:
Title
Asthma Control Days
Description
proportion of study days on which asthma was controlled, measured by electronic diary
Time Frame
last 46 weeks of 48 week treatment period
Title
Asthma Rescue Medication Use
Description
average albuterol rescue use per week, measured by electronic diary
Time Frame
last 46 weeks of 48 week treatment period
Title
Health Care Utilization
Description
frequency of unscheduled physician visits, emergency department visits or hospitalizations for asthma
Time Frame
last 46 weeks of 48 week treatment period

10. Eligibility

Sex
All
Minimum Age & Unit of Time
12 Months
Maximum Age & Unit of Time
59 Months
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 12-59 months of age. If the child is not currently taking long-term asthma controller therapy (meaning that the child has taken no inhaled corticosteroid or leukotriene receptor antagonist medication whatsoever over the past 6 months), then one of the following criteria must be met: Daytime asthma symptoms more than two days per week (average over the past 4 weeks), At least one nighttime awakening from asthma (over the past 4 weeks), Two or more asthma exacerbations requiring systemic corticosteroids in the previous 6 months, Four or more wheezing episodes in the previous 12 months. If the child is currently taking long-term asthma controller therapy (meaning that the child has taken daily or intermittent/as-needed inhaled corticosteroid or leukotriene receptor antagonist over the past 6 months), then one of the following criteria must be met: Taking inhaled corticosteroid or leukotriene receptor antagonist for more than 3 months (or more than 90 days) out of the previous 6 months (or 180 days), Daytime asthma symptoms more than two days per week (average over the past 4 weeks), More than one nighttime awakening from asthma (over the past 4 weeks), Two or more asthma exacerbations requiring systemic corticosteroids in the previous 12 months, Four or more wheezing episodes in the previous 12 months. Up to date with immunizations, including varicella (unless the subject has already had clinical varicella). Willingness to provide informed consent by the child's parent or guardian. Exclusion Criteria: Allergic reaction to the study medications or any component of the study drugs, including (but not limited to) urticaria, rash, angioedema, or hypotension following delivery, Chronic medical disorders that could interfere with drug metabolism/excretion (for instance chronic hepatic, biliary, or renal disease), Chronic medical disorders that may increase the risk of drug-related injury, including (but not limited to): Osteogenesis imperfecta (increased risk of bone demineralization/fracture with corticosteroid therapy), Crohn's disease, ulcerative colitis, juvenile rheumatoid arthritis, clotting disorders, or Factor deficiency (increased risk of bleeding with corticosteroid therapy), G6PD deficiency (increased risk of hemolytic anemia with acetaminophen use), Phenylketonuria (potential for aspartame exposure with study interventions), Seizure disorder treated with anticonvulsants (risk of acetaminophen toxicity with carbamazepine), or History of clotting disorders or Factor deficiency (increased risk of bleeding with corticosteroids), Co-morbid disorders associated with wheezing including (but not limited to) immune deficiency disorders, cystic fibrosis, aspiration, clinically-relevant gastroesophageal reflux, tracheomalacia, congenital airway anomalies (clefts, fistulas, slings, rings), bronchiectasis, bronchopulmonary dysplasia, and/or history of premature birth before 35 weeks gestation, Significant developmental delay/failure to thrive, defined as 5th percentile for height and/or weight or crossing of two major percentile lines during the last year for age and sex, History of a near-fatal asthma exacerbation requiring intubation or assisted ventilation, No primary medical caregiver (e.g., a nurse practitioner, physician assistant, physician, or group medical practice such as a hospital-based clinic) whom the subject can contact for primary medical care, Three or more hospitalizations in the previous 12 months for wheezing or respiratory illnesses, Treatment with 5 or more courses of systemic corticosteroids (oral, intramuscular or intravenous) in the past 6 months, Current use of higher than step 2 NAEPP asthma guideline therapy If receiving allergy shots, change in the dose within the past 3 months.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
William B Busse, MD
Organizational Affiliation
University of Wisconsin, Madison
Official's Role
Study Chair
Facility Information:
Facility Name
University of Arizona College of Medicine
City
Tucson
State/Province
Arizona
ZIP/Postal Code
85724
Country
United States
Facility Name
Children's Hospital & Research Center Oakland
City
Oakland
State/Province
California
ZIP/Postal Code
94609
Country
United States
Facility Name
UCSF Benioff Children's Hospital
City
San Francisco
State/Province
California
ZIP/Postal Code
94143
Country
United States
Facility Name
National Jewish Health
City
Denver
State/Province
Colorado
ZIP/Postal Code
80206
Country
United States
Facility Name
Emory University
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30322
Country
United States
Facility Name
Rush University Medical Center/Stroger Hospital
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60612
Country
United States
Facility Name
Children's Memorial Hospital
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60614
Country
United States
Facility Name
Children's Hospital Boston
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02115
Country
United States
Facility Name
Children's Hospital, Boston
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02115
Country
United States
Facility Name
St. Louis Children's Hospital
City
St. Louis
State/Province
Missouri
ZIP/Postal Code
63110
Country
United States
Facility Name
Wake Forest University Health Sciences
City
Winston-Salem
State/Province
North Carolina
ZIP/Postal Code
27157
Country
United States
Facility Name
Rainbow Babies and Children's Hospital, Case Western Reserve University
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44106
Country
United States
Facility Name
Children's Hospital of Pittsburgh of UPMC
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15224
Country
United States
Facility Name
University of Virginia Health System
City
Charlottesville
State/Province
Virginia
ZIP/Postal Code
22908
Country
United States
Facility Name
University of Wisconsin-Madison
City
Madison
State/Province
Wisconsin
ZIP/Postal Code
53792
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
27532828
Citation
Sheehan WJ, Mauger DT, Paul IM, Moy JN, Boehmer SJ, Szefler SJ, Fitzpatrick AM, Jackson DJ, Bacharier LB, Cabana MD, Covar R, Holguin F, Lemanske RF Jr, Martinez FD, Pongracic JA, Beigelman A, Baxi SN, Benson M, Blake K, Chmiel JF, Daines CL, Daines MO, Gaffin JM, Gentile DA, Gower WA, Israel E, Kumar HV, Lang JE, Lazarus SC, Lima JJ, Ly N, Marbin J, Morgan WJ, Myers RE, Olin JT, Peters SP, Raissy HH, Robison RG, Ross K, Sorkness CA, Thyne SM, Wechsler ME, Phipatanakul W; NIH/NHLBI AsthmaNet. Acetaminophen versus Ibuprofen in Young Children with Mild Persistent Asthma. N Engl J Med. 2016 Aug 18;375(7):619-30. doi: 10.1056/NEJMoa1515990.
Results Reference
derived

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Acetaminophen Versus Ibuprofen in Children With Asthma

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