Individualized Therapy For Asthma in Toddlers (INFANT)
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Purpose
The INFANT study will test whether, in preschool children 12-59 months of age with persistent asthma, the following Step 2 asthma therapies will provide similar degrees of asthma control:
- Daily inhaled corticosteroid (ICS) treatment,
- Daily leukotriene receptor antagonist (LTRA) treatment, and
- As-needed ICS plus short-acting beta agonist (as-needed ICS/SABA) rescue treatment.
| Condition | Intervention | Phase |
|---|---|---|
|
Asthma Wheezing |
Drug: daily fluticasone propionate Drug: Montelukast Drug: as-needed fluticasone propionate |
Phase 3 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Crossover Assignment Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor) Primary Purpose: Treatment |
| Official Title: | Individualized Therapy For Asthma in Toddlers |
- Differential Response to the Three Therapies Based on Fixed Threshold Criteria for the Following Asthma Control Measures: Use of Oral Prednisone for Acute Asthma Exacerbations and Asthma Control Days. [ Time Frame: The last 14 weeks of each 16-week treatment period ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 294 |
| Study Start Date: | February 2013 |
| Estimated Study Completion Date: | January 2015 |
| Estimated Primary Completion Date: | January 2015 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: Crossover sequence 1
daily fluticasone propionate, followed by daily montelukast, followed by as needed fluticasone propionate
|
Drug: daily fluticasone propionate
Flovent® HFA, 44 mcg per inhalation, 2 inhalations twice daily
Drug: Montelukast
Singulair®, 4 mg granules or chewable tablets by mouth once daily in the evening
Drug: as-needed fluticasone propionate
Flovent® HFA, 44 mcg per inhalation, 2 inhalations, as needed for asthma symptoms
|
|
Experimental: Crossover sequence 2
daily fluticasone propionate, followed by as needed fluticasone propionate, followed by daily montelukast
|
Drug: daily fluticasone propionate
Flovent® HFA, 44 mcg per inhalation, 2 inhalations twice daily
Drug: Montelukast
Singulair®, 4 mg granules or chewable tablets by mouth once daily in the evening
Drug: as-needed fluticasone propionate
Flovent® HFA, 44 mcg per inhalation, 2 inhalations, as needed for asthma symptoms
|
|
Experimental: Crossover sequence 3
daily montelukast, followed by as needed fluticasone propionate, followed by daily fluticasone propionate
|
Drug: daily fluticasone propionate
Flovent® HFA, 44 mcg per inhalation, 2 inhalations twice daily
Drug: Montelukast
Singulair®, 4 mg granules or chewable tablets by mouth once daily in the evening
Drug: as-needed fluticasone propionate
Flovent® HFA, 44 mcg per inhalation, 2 inhalations, as needed for asthma symptoms
|
|
Experimental: Crossover sequence 4
daily montelukast, followed by daily fluticasone propionate, followed by as needed fluticasone propionate
|
Drug: daily fluticasone propionate
Flovent® HFA, 44 mcg per inhalation, 2 inhalations twice daily
Drug: Montelukast
Singulair®, 4 mg granules or chewable tablets by mouth once daily in the evening
Drug: as-needed fluticasone propionate
Flovent® HFA, 44 mcg per inhalation, 2 inhalations, as needed for asthma symptoms
|
|
Experimental: Crossover sequence 5
as needed fluticasone propionate, followed by daily fluticasone propionate, followed by daily montelukast
|
Drug: daily fluticasone propionate
Flovent® HFA, 44 mcg per inhalation, 2 inhalations twice daily
Drug: Montelukast
Singulair®, 4 mg granules or chewable tablets by mouth once daily in the evening
Drug: as-needed fluticasone propionate
Flovent® HFA, 44 mcg per inhalation, 2 inhalations, as needed for asthma symptoms
|
|
Experimental: Crossover sequence 6
as needed fluticasone propionate, followed by daily montelukast, followed by daily fluticasone propionate
|
Drug: daily fluticasone propionate
Flovent® HFA, 44 mcg per inhalation, 2 inhalations twice daily
Drug: Montelukast
Singulair®, 4 mg granules or chewable tablets by mouth once daily in the evening
Drug: as-needed fluticasone propionate
Flovent® HFA, 44 mcg per inhalation, 2 inhalations, as needed for asthma symptoms
|
Detailed Description:
INFANT is a double-blind, randomized clinical trial in which all participants will receive each of the three therapies for 16 weeks by means of a cross-over study design. INFANT aims to determine whether individual children respond better to one treatment than another and, if so, whether those children can be identified by phenotypic characteristics or selected biomarkers. In this regard the INFANT study is expected to address critical gaps in current asthma management guidelines. Ultimately, the findings from this study are expected to help clarify treatment modalities for this population of young preschool children who are extremely difficult to treat.
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 | 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 | |
| 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, 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: | NCT01606306 History of Changes |
| Other Study ID Numbers: | AsthmaNet 004, 1U10HL098115 |
| Study First Received: | May 23, 2012 |
| Last Updated: | February 25, 2013 |
| Health Authority: | United States: Food and Drug Administration United States: Federal Government |
Keywords provided by Milton S. Hershey Medical Center:
|
Asthma Wheezing Fluticasone Montelukast Preschool-age |
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 Fluticasone Montelukast |
Bronchodilator Agents Autonomic Agents Peripheral Nervous System Agents Physiological Effects of Drugs Pharmacologic Actions Anti-Asthmatic Agents Respiratory System Agents Therapeutic Uses Dermatologic Agents Anti-Allergic Agents Anti-Inflammatory Agents Leukotriene Antagonists Hormone Antagonists Hormones, Hormone Substitutes, and Hormone Antagonists |
ClinicalTrials.gov processed this record on May 16, 2013