An Open-label Study to Evaluate Correct Use and Ease of Use of the ELLIPTA DPI in Pediatric Subjects With Asthma

Completed · Phase 4 · Has a placebo group

Conditions studied: Asthma

In brief

Asthma is a chronic inflammatory disease of airways and lungs that results in hyper-reactivity and clinically relevant episodes of wheezing. This study has been designed to assess the correct use and ease of use of the ELLIPTA® DPI in pediatric subjects with asthma. ELLIPTA DPI is easy to use, requires few steps, is consistent in dosing and eliminates the hand-breath co-ordination required for metered dose inhalers (MDIs). Subjects will be stratified by age into two strata: Stratum 1: subjects in the age group of 5 to 7 years and Stratum 2: Subjects in the age group of 8 to 11 years. All subjects will be trained by Health care professionals (HCP) for the correct use of ELLIPTA DPI. Subjects will be given three chances to attempt correct use of ELLIPTA DPI; subsequently, if the subject is not successful, the parent/guardian will be able to help instruct the subject on the correct use of the ELLIPTA DPI, for two more attempts. The subjects who will be enrolled in the study will take placebo ELLIPTA DPI once daily. After 28 days subjects will be randomized in 1:1 to receive a questionnaire (Version A and B). After completion of the questionnaire on ELLIPTA DPI ease of use, subject's ability to use ELLIPTA DPI correctly will be re-assessed. Approximately 219 subjects will be screened to participate in the study. The study will be conducted for 28 days. ELLIPTA is a registered trademark of GlaxoSmithKline (GSK) group of companies.

Key facts

Study ID: NCT03478657
Run by: GlaxoSmithKline
People needed: 222
Starts: 2018-06-18
Expected to finish: 2018-12-07
Last updated by the study team: 2021-03-26

Who can join

Age: 5 and older, up to 11. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

Subjects between 5 and 11 years old (inclusive), at the time of the Visit 0.
Subjects with a documented history of symptoms consistent with a diagnosis of asthma for at least 6 months prior to V0 (includes asthma diagnosis).
Males and premenarchial females.
Written informed consent from at least one parent/guardian and the accompanying informed assent from the subject (where the subject is able to provide assent) prior to admission to the study.
Subject and their legal guardian understand and are willing, able, and likely to comply with study procedures and assessments.
Subject must have been receiving asthma treatment (rescue or maintenance) for 3 months prior to entry onto the study.
Subject must have never been trained in correct use of, or used the ELLIPTA DPI previously.
Subjects must be able to demonstrate correct use of the ELLIPTA DPI after coaching/training at Visit 1.
Subjects must be able to converse and understand verbal instruction in English.

You may not qualify if…

Subjects with concurrent diagnosis of other respiratory disorders including active tuberculosis, lung cancer, bronchiectasis, sarcoidosis, lung fibrosis, pulmonary hypertension, interstitial lung diseases, cystic fibrosis or other active pulmonary diseases.
Subjects with concurrent diagnosis of psychiatric or psychological or any other disorders that in the opinion of the investigator may affect the ability of the subject to comply with study procedures or requirements.
Subject has experienced an exacerbation which required oral/systemic corticosteroids in the three months prior to Visit 0.
Subject has been hospitalized for an episode of asthma within three months of Visit 0.
Subject has had an asthmatic episode requiring intubation, associated with hypercapnia, respiratory arrest or hypoxic seizures.
Subject has exhibited symptoms of a recent acute respiratory tract infection within one week of Visit 0.
Subject has history of hypersensitivity to any components of the study inhalers (example [e.g.], lactose, magnesium stearate). In addition, subjects with a history of severe milk protein allergy that, in the opinion of the study physician, contraindicates participation will also be excluded.
Subjects with historical or current evidence of clinically significant or rapidly progressing or unstable cardiovascular, neurological, renal, hepatic, immunological, endocrine (including diabetes or thyroid disease) or hematological abnormalities that are uncontrolled. Significant is defined as any disease that, in the opinion of the investigator, would put the safety of the subject at risk through participation, or which would affect the analysis if the disease/condition exacerbated during the study.
Parent or Guardian with a history of psychiatric disease, intellectual deficiency, substance abuse or other condition (e.g. inability to read, comprehend or write) which may affect: Validity of consent to participate in the study; Adequate supervision of the subject during the study; Compliance of subject with study medication and study procedures; subject safety and well-being.
Subjects who have received an investigational drug and/or medical device within 30 days of entry into this study (Screening), or within five drug half-lives of the investigational drug, whichever is longer.
A subject will not be eligible for this study if he/she is an immediate family member of the participating investigator, sub-investigator, study coordinator, or employee of the participating investigator.

Where it is running

GSK Investigational Site — Little Rock, Arkansas, United States
GSK Investigational Site — Huntington Beach, California, United States
GSK Investigational Site — Napa, California, United States
GSK Investigational Site — Aventura, Florida, United States
GSK Investigational Site — Miami, Florida, United States
GSK Investigational Site — Plantation, Florida, United States
GSK Investigational Site — Owensboro, Kentucky, United States
GSK Investigational Site — Minneapolis, Minnesota, United States
GSK Investigational Site — Plymouth, Minnesota, United States
GSK Investigational Site — Columbia, Missouri, United States
GSK Investigational Site — Rolla, Missouri, United States
GSK Investigational Site — Asheville, North Carolina, United States
GSK Investigational Site — Summerville, South Carolina, United States
GSK Investigational Site — Austin, Texas, United States
GSK Investigational Site — Waco, Texas, United States
GSK Investigational Site — Brampton, Ontario, Canada
GSK Investigational Site — Burlington, Ontario, Canada
GSK Investigational Site — London, Ontario, Canada
GSK Investigational Site — Windsor, Ontario, Canada

Full record on ClinicalTrials.gov

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