Acetaminophen Versus Ibuprofen in Children With Asthma (AVICA)
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Purpose
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.
| Condition | Intervention | Phase |
|---|---|---|
|
Asthma Wheezing |
Drug: Acetaminophen Drug: Ibuprofen |
Phase 3 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor) Primary Purpose: Treatment |
| Official Title: | Acetaminophen vs. Ibuprofen in Children With Asthma |
- exacerbation frequency [ Time Frame: 48 week treatment period ] [ Designated as safety issue: No ]the number of asthma exacerbations requiring systemic corticosteroids
| Estimated Enrollment: | 294 |
| Study Start Date: | February 2013 |
| Estimated Study Completion Date: | February 2015 |
| Estimated Primary Completion Date: | February 2015 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: acetaminophen
acetaminophen given as needed for pain or fever
|
Drug: Acetaminophen
15 mg/kg every 6 hours as needed
Other Names:
|
|
Experimental: ibuprofen
ibuprofen given as needed for pain or fever
|
Drug: Ibuprofen
9.4 mg/kg every 6 hours as needed
Other Names:
|
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.
Eligibility| Ages Eligible for Study: | 12 Months to 59 Months |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
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.
Contacts and Locations| Contact: David T Mauger, PhD | 717.531.7178 | dtm5@psu.edu |
| United States, Arizona | |
| University of Arizona College of Medicine | Recruiting |
| Tucson, Arizona, United States, 85724 | |
| United States, California | |
| Children's Hospital & Research Center Oakland | Recruiting |
| Oakland, California, United States, 94609 | |
| UCSF Benioff Children's Hospital | Recruiting |
| San Francisco, California, United States, 94143 | |
| United States, Colorado | |
| National Jewish Health | Recruiting |
| Denver, Colorado, United States, 80206 | |
| United States, Georgia | |
| Emory University | Recruiting |
| Atlanta, Georgia, United States, 30322 | |
| Contact: Denise Whitlock 404-712-1773 drwhitl@emory.edu | |
| United States, Illinois | |
| Children's Memorial Hospital | Recruiting |
| Chicago, Illinois, United States, 60614 | |
| Rush University Medical Center/Stroger Hospital | Recruiting |
| Chicago, Illinois, United States, 60612 | |
| United States, Massachusetts | |
| Children's Hospital Boston | Recruiting |
| Boston, Massachusetts, United States, 02115 | |
| Children's Hospital, Boston | Recruiting |
| Boston, Massachusetts, United States, 02115 | |
| Contact: Jennifer Truong 857-218-5138 jennifer.truong@childrens.harvard.edu | |
| United States, Missouri | |
| St. Louis Children's Hospital | Recruiting |
| St. Louis, Missouri, United States, 63110 | |
| United States, North Carolina | |
| Wake Forest University Health Sciences | Recruiting |
| Winston-Salem, North Carolina, United States, 27157 | |
| United States, Ohio | |
| Rainbow Babies and Children's Hospital, Case Western Reserve University | Recruiting |
| Cleveland, Ohio, United States, 44106 | |
| Contact: Laurie Logan 216-844-7927 Laurie.Logan@UHhospitals.org | |
| United States, Pennsylvania | |
| Children's Hospital of Pittsburgh of UPMC | Recruiting |
| Pittsburgh, Pennsylvania, United States, 15224 | |
| United States, Virginia | |
| University of Virginia Health System | Recruiting |
| Charlottesville, Virginia, United States, 22908 | |
| United States, Wisconsin | |
| University of Wisconsin-Madison | Recruiting |
| Madison, Wisconsin, United States, 53792 | |
| Study Chair: | William B Busse, MD | University of Wisconsin, Madison |
More Information
No publications provided
| Responsible Party: | dave mauger, Principal Investigator, AsthmaNet Data Coordinating Center, Milton S. Hershey Medical Center |
| ClinicalTrials.gov Identifier: | NCT01606319 History of Changes |
| Other Study ID Numbers: | AsthmaNet 005, 1U10HL098115 |
| Study First Received: | May 23, 2012 |
| Last Updated: | March 1, 2013 |
| Health Authority: | United States: Institutional Review Board United States: Federal Government |
Keywords provided by Milton S. Hershey Medical Center:
|
Asthma Wheezing Ibuprofen Acetaminophen |
exacerbations pain fever |
Additional relevant MeSH terms:
|
Asthma Respiratory Sounds Bronchial Diseases Respiratory Tract Diseases Lung Diseases, Obstructive Lung Diseases Respiratory Hypersensitivity Hypersensitivity, Immediate Hypersensitivity Immune System Diseases Signs and Symptoms, Respiratory Signs and Symptoms Acetaminophen Ibuprofen Anti-Inflammatory Agents |
Anti-Inflammatory Agents, Non-Steroidal Antipyretics Physiological Effects of Drugs Pharmacologic Actions Analgesics, Non-Narcotic Analgesics Sensory System Agents Peripheral Nervous System Agents Central Nervous System Agents Therapeutic Uses Antirheumatic Agents Cyclooxygenase Inhibitors Enzyme Inhibitors Molecular Mechanisms of Pharmacological Action |
ClinicalTrials.gov processed this record on May 21, 2013