Acetaminophen Versus Ibuprofen in Children With Asthma

NCT ID: NCT01606319

Last Updated: 2017-01-16

Study Results

Results available

Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.

View full results

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

PHASE3

Total Enrollment

300 participants

Study Classification

INTERVENTIONAL

Study Start Date

2013-02-28

Study Completion Date

2015-04-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

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.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Asthma Wheezing

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

QUADRUPLE

Participants Caregivers Investigators Outcome Assessors

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

acetaminophen

acetaminophen given as needed for pain or fever

Group Type EXPERIMENTAL

Acetaminophen

Intervention Type DRUG

15 mg/kg every 6 hours as needed

ibuprofen

ibuprofen given as needed for pain or fever

Group Type EXPERIMENTAL

Ibuprofen

Intervention Type DRUG

9.4 mg/kg every 6 hours as needed

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Acetaminophen

15 mg/kg every 6 hours as needed

Intervention Type DRUG

Ibuprofen

9.4 mg/kg every 6 hours as needed

Intervention Type DRUG

Other Intervention Names

Discover alternative or legacy names that may be used to describe the listed interventions across different sources.

tylenol paracetamol motrin advil nonsteroidal anti-inflammatory drug

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

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.
Minimum Eligible Age

12 Months

Maximum Eligible Age

59 Months

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

National Heart, Lung, and Blood Institute (NHLBI)

NIH

Sponsor Role collaborator

Milton S. Hershey Medical Center

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

dave mauger

Principal Investigator, AsthmaNet Data Coordinating Center

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

William B Busse, MD

Role: STUDY_CHAIR

University of Wisconsin, Madison

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

University of Arizona College of Medicine

Tucson, Arizona, United States

Site Status

Children's Hospital & Research Center Oakland

Oakland, California, United States

Site Status

UCSF Benioff Children's Hospital

San Francisco, California, United States

Site Status

National Jewish Health

Denver, Colorado, United States

Site Status

Emory University

Atlanta, Georgia, United States

Site Status

Rush University Medical Center/Stroger Hospital

Chicago, Illinois, United States

Site Status

Children's Memorial Hospital

Chicago, Illinois, United States

Site Status

Children's Hospital Boston

Boston, Massachusetts, United States

Site Status

Children's Hospital, Boston

Boston, Massachusetts, United States

Site Status

St. Louis Children's Hospital

St Louis, Missouri, United States

Site Status

Wake Forest University Health Sciences

Winston-Salem, North Carolina, United States

Site Status

Rainbow Babies and Children's Hospital, Case Western Reserve University

Cleveland, Ohio, United States

Site Status

Children's Hospital of Pittsburgh of UPMC

Pittsburgh, Pennsylvania, United States

Site Status

University of Virginia Health System

Charlottesville, Virginia, United States

Site Status

University of Wisconsin-Madison

Madison, Wisconsin, United States

Site Status

Countries

Review the countries where the study has at least one active or historical site.

United States

References

Explore related publications, articles, or registry entries linked to this study.

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.

Reference Type DERIVED
PMID: 27532828 (View on PubMed)

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

1U10HL098115

Identifier Type: NIH

Identifier Source: secondary_id

View Link

AsthmaNet 005

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Asthma in Children
NCT01286532 COMPLETED
Montelukast With Status Asthmaticus, Ages 6-18
NCT00494572 UNKNOWN PHASE2/PHASE3
Dose-response of Albuterol in Asthmatics
NCT00940927 COMPLETED PHASE4