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Phase 2 N=155 Randomized Treatment

Environmental Control as Add-on Therapy in Childhood Asthma

Asthma

Enrolled (actual)
155
Serious AEs
7.7%
Results posted
Nov 2019
Primary outcome: Primary: The Medication Treatment Step Assigned — 4.03; 4.05 score on a scale

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
Flovent Diskus (Drug); Home Environmental Intervention (Other); Advair Diskus (Drug)
Age
Pediatric · 5+ yrs
Sex
All
Sponsor
Johns Hopkins University
Primary completion
Nov 2018

Outcome Measures

OutcomeResultp-value
PRIMARY
The Medication Treatment Step Assigned
4.03; 4.05
SECONDARY
Daily Inhaled Corticosteroid Dose
557.5; 527.7
SECONDARY
Exhaled Nitric Oxide
20; 20
SECONDARY
Number of Asthma Symptom Days
2.5; 2.7
SECONDARY
Number of Asthma Exacerbations
35; 53
SECONDARY
FEV1/FVC
79.3; 80.8

Summary

This study evaluates the effects of adding on an environmental home intervention to standard asthma medication management on controller medication requirements among children and adolescents with asthma. The investigators hypothesize that the addition of an individually-tailored, multi-faceted Environmental Control Strategy (ECS) to guidelines-based controller medication will result in less controller medication requirement and allergic inflammation than controller medication alone among urban asthmatic children.

Eligibility Criteria

Inclusion Criteria

  • Have physician-diagnosed asthma at least 1 year prior to the baseline visit, or asthma symptoms for at least 1 year
  • Meet criteria for current persistent asthma defined as either:
  • On a long-term controller medication for asthma, or
  • Meet National Asthma Education and Prevention Program (NAEPP) guideline requirements for persistent disease:(46)
  • Asthma symptoms 3 or more days per week over the past 2 weeks or
  • Nocturnal asthma symptoms at least 3 times in the past month
  • Have evidence of uncontrolled disease as defined by at least one of the following:
  • One asthma-related unscheduled visit to an emergency department (ED), clinic or urgent care facility in the previous 12 mo
  • One asthma-related overnight hospitalization in the previous 12 mo
  • One or more bursts of oral corticosteroids in the previous 12 mo
  • Reside within a geographic area of the study site so that home visits are feasible.
  • Have no plans to move within the upcoming 6 months
  • Have insurance to cover prescription medications.
  • Have a positive skin test (net wheal ≥2mm) to cat, dog, mouse, cockroach, or dust mites or have a positive cat, dog, mouse, German cockroach, or D. farinae-specific immunoglobulin E (IgE) test, as quantified using the ImmunoCAP system (≥0.35 kU/L)

Exclusion Criteria

  • Lung disease, other than asthma, that requires daily medication
  • Cardiovascular disease that requires daily medication, excluding hypertension
  • Taking a beta-blocker
  • Allergy to dairy
  • On Xolair < 5 months
  • On immunotherapy and has not reached maintenance dose
  • Sleeping in another home 4 or more nights/week
  • Active smoker defined as a positive urine screen for high levels of urine cotinine
  • Unable to access areas of home necessary to conduct extermination
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02251379). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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