Sunovion Growth Study Pediatric Subjects With Mild Asthma & Allergic Rhinitis

Completed · Phase 4 · Has a placebo group

Conditions studied: Asthma, Allergic Rhinitis

In brief

This study will provide the clinicians guidance on the safest combination of inhaled and nasal corticosteroids for children with mild asthma and allergic rhinitis respectively; however, one safety concern is that these products are independently known to have dose-related effects on short term and intermediate term growth. Knemometry is a non invasive technique for measuring short-term lower leg growth in children and is currently the method of choice in growth studies of short duration. Subjects will be seen on a weekly basis for 18 weeks and at each visit, lower leg length will be measured using knemometry.

Key facts

Study ID

NCT01550471

Run by

West Penn Allegheny Health System

People needed

22

Starts

2012-03-01

Expected to finish

2015-08-01

Last updated by the study team

2020-11-04

Who can join

Age: 6 and older, up to 15. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Subjects will include females and males 6 to 15 years of age.
• All subjects must have a history of physician diagnosed mild asthma and allergic rhinitis as documented by PCP medical record or detailed history by study investigator.
• All subjects must have a height within normal limits (5th to 95th percentile) and no history of abnormal growth as assessed by medical history.
• Subjects may be on current treatment with montelukast as this drug does not affect growth. If a subject is on montelukast at screening/baseline, they will remain on a stable dose throughout the study.
• Subjects must be willing to comply with study requirements.

You may not qualify if…

• Subjects will be excluded if they have asthma greater than mild persistent severity as defined by NHLBI guidelines.
• 2 Subjects will be excluded if they used any systemic steroids within the past 60 days.
• Subjects will be excluded if they had more than one burst of systemic steroids within the past year.
• Subjects will be excluded if their baseline FEV1 is < 80% predicted. 5. Subjects will be excluded if they have any other serious systemic disease other than asthma.
• Subjects will be excluded if they have taken any medication known to affect growth i.e. ADHD medications within the past 60 days 7. Subjects will be excluded if they have a history of allergy to any of the study medications.
• Subjects will be excluded if they have active chickenpox or measles or recent exposure to chickenpox or measles.
• Subjects will be excluded if they have any history of tuberculosis of the respiratory tract.
• Subjects will be excluded if they have any active fungal, bacterial, viral or parasitic infections.
• Subjects will be excluded if they have any history of herpes simplex infection of the eye.
• Subjects will be excluded if they have taken any immunosuppressive drugs within the past 2 months.
• Subjects will be excluded if they have any history of Churg-Strauss syndrome or other eosinophilic disorders.
• Subjects will be excluded if an investigator deems they have any mental or development health issues, such as autism, moderate to severe mental retardation or severe ADHD, that interferes with their ability to complete the knemometry measurements.
• Subjects will be excluded if an investigator deems they have any physical issues, such as inability to sit independently or amputation of lower leg, that interferes with their ability to complete the knemometry measurements.

Where it is running

• Pediatric Alliance-Greentree Division — Green Tree, Pennsylvania, United States
• Alleghney General Hospital — Pittsburgh, Pennsylvania, United States

Full record on ClinicalTrials.gov

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