Last updated: 07/17/2024 17:30:49
A clinical study assessing critical errors, training/teaching time, and preference attributes of the ELLIPTA® dry powder inhaler, in comparison to combinations of dry powder inhalers used to provide triple therapy, in patients with Chronic Obstructive Pulmonary Disease
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Study complete
Study complete
Trial overview
Official title: A randomized, open-label, cross-over, placebo-device study investigating critical and over all errors, training/teaching time, and preference attributes of the ELLIPTA dry powder Inhaler (DPI) as compared to HANDIHALER DPI used in combination with either DISKUS DPI or TURBUHALER DPI, in adult patients with Chronic Obstructive Pulmonary Disease (COPD)
Trial description: This is a randomized, multi-centre, open-label, placebo-device, cross-over study, with a 2x2 complete block design in subjects with chronic obstructive pulmonary disease (COPD) to assess the benefits of delivering triple therapy using a single ELLIPTA dry powder inhaler (DPI) (closed triple therapy) versus delivering triple therapy using two different types of DPI (open triple therapy). The primary objective of the study is to evaluate the proportion of COPD subjects who make critical errors when using a single ELLIPTA DPI versus those using combinations of DISKUS® with HANDIHALER®, or TURBUHALER® with HANDIHALER. At Visit 1, all subjects will demonstrate the use of ELLIPTA DPI, and HANDIHALER DPI in combination with either DISKUS DPI (in sub-study 1) or TURBUHALER DPI (in sub-study 2), based on the treatment sequences. At the end Visit 1, subjects will complete the inhaler preference questionnaire (PQ). There is no active treatment and subjects will continue to take their own prescribed COPD medication for the duration of the study. ELLIPTA and DISKUS are registered trademarks of the GSK group of companies; TURBUHALER is a registered trademark of AstraZeneca and HANDIHALER is a registered trademark of Boehringer Ingelheim Pharma GmbH & Co. KG.
Primary purpose:
Treatment
Trial design:
Crossover Assignment
Masking:
None (Open Label)
Allocation:
Randomized
Primary outcomes:
Percentage of participants making at least one critical error after reading the patient information leaflets (PIL)
Timeframe: Day 1
Secondary outcomes:
Percentage of participants making at least one critical error after the first instruction from the HCP
Timeframe: Day 1
Percentage of participants making at least one critical error after the second instruction from the HCP
Timeframe: Day 1
Percentage of participants making at least one overall error after reading the PIL
Timeframe: Day 1
Percentage of participants making at least one overall error after the first instruction from the HCP
Timeframe: Day 1
Percentage of participants making at least one overall error after the second instruction from the HCP
Timeframe: Day 1
Number of participants with instructions (0, 1 or 2 times) from the HCP which are needed to demonstrate correct inhaler use
Timeframe: Day 1
The median time to demonstrate correct inhaler use (T1+T2)
Timeframe: Day 1
Time taken to read the PIL and demonstrate correct inhaler use (T1)
Timeframe: Day 1
Time taken to be given instruction by the HCP (up to 2 times) on use of the inhaler and to demonstrate correct inhaler use (T2)
Timeframe: Day 1
Number of participants with treatment preference based on responses to the preference questionnaire, which considered the number of steps required to take the COPD medication
Timeframe: Day 1
Number of participants with treatment preference based on responses to the preference questionnaire, which considered overall treatment preference
Timeframe: Day 1
Interventions:
Enrollment:
160
Primary completion date:
2017-19-06
Observational study model:
Not applicable
Time perspective:
Not applicable
Clinical publications:
Job Van Der Palen, Wendy Moeskops-Van Beurden, Carolyn Dawson, Wai-Yee James, Andy Preece, Dawn Midwinter, Neil Barnes, Raj Sharma. A randomized, open-label, single-visit crossover study simulating triple-drug delivery with Ellipta compared with dual inhaler combinations in patients with COPD. Int J Chron Obstruct Pulmon Dis. 2018;13:2515—2523.
DOI: 10.2147/COPD.S169060
Medical condition
Pulmonary Disease, Chronic Obstructive
Product
fluticasone furoate, fluticasone furoate/vilanterol/umeclidinium bromide, umeclidinium bromide, vilanterol
Collaborators
Not applicable
Study date(s)
December 2016 to June 2017
Type
Interventional
Phase
4
Participation criteria
Sex
Female & Male
Age
40+ years
Accepts healthy volunteers
No
- Inclusion Criteria
- Age >=40 years at Visit 1
Inclusion and exclusion criteria
Inclusion criteria:
- Inclusion Criteria
- Age >=40 years at Visit 1
- Diagnosis of COPD with a documented history of COPD, in accordance with the definition by the European Respiratory Society.
- Current COPD Therapy: Currently receiving maintenance therapy with a fixed dose combination of a long-acting beta 2-agonist (LABA) and inhaled corticosteroid (ICS). Subject may also be receiving long-acting muscarinic antagonist (LAMA; also known as a long-acting anti-cholinergic). Subjects must be able to continue using their currently prescribed COPD maintenance inhaler therapy throughout the study and as needed short acting beta-adrenergic agonist (SABA) and/or short acting muscarinic antagonist (SAMA) for rescue use.
- Has been on current maintenance ICS/LABA COPD treatment for at least 4 weeks prior to V0 and evaluated as unlikely to change treatment within 4 weeks of Visit 1.
- Current or former (defined as subjects who have quit smoking for at least 3 months prior to V0/V1) cigarette smokers with a >10 pack-year smoking history (Number of pack years=[number of cigarettes per day ÷ 20] x number of years smoked [e.g., 10 pack-years is equal to 20 cigarettes per day for 10 years, or 10 cigarettes per day for 20 years]).
- Males or females who are not pregnant or not planning a pregnancy during the study or not lactating
- Capable of giving signed informed consent which includes compliance with the requirements and restrictions listed in the informed consent form (ICF) and in this protocol. Exclusion Criteria
- Subjects with a current diagnosis of asthma. Subjects with a prior history of asthma are eligible if they have a current diagnosis of COPD.
- Subjects who used any ELLIPTA inhaler (participated in a clinical study of GW685698, GW642444, GSK573719 [fluticasone furoate, vilanterol, umeclidinium bromide], or any combination thereof, or placebo in an ELLIPTA inhaler study) within 24 months prior to Visit 0.
- Subjects who used any capsule system inhaler (e.g. Spiriva HANDIHALER, SEEBRI®/ULTIBRO® BREEZHALER®, or participated in a clinical studies of these, including placebo inhalers) within 24 months prior to Visit 0. SEEBRI, ULTIBRO, and BREEZHALER are registered trademarks of Novartis AG.
- Dependent on which sub-study a subject is included on they should not have any recent experience, within 24 months of V 0 of the following inhaler for the sub study included on: Sub Study 1: DISKUS inhaler (e.g., Seretide DISKUS or placebo DISKUS) and Sub Study 2:TURBUHALER (e.g. Symbicort TURBUHALER or placebo TURBUHALER)
- Subjects with a known or suspected alcohol or drug abuse at Visit 1 which in the opinion of the investigator could interfere with the subject’s proper completion of the protocol requirement
- A history of hypersensitivity to any components of the study inhaler (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 who have received an investigational drug and/or medical device within 30 days of entry into this study (Screening/Visit 1), or within five drug half-lives of the investigational drug, whichever is longer
- In the opinion of the investigator, any subject who is unable to read and/or would not be able to complete a questionnaire and understand verbal instructions.
Trial location(s)
Study documents
Protocol
Available language(s): English
Statistical analysis plan
Available language(s): English
Clinical study report
Available language(s): English
If you wish to request for full study report, please contact - [email protected]
Results overview
Results posted on ClinicalTrials.gov
Recruitment status
Study complete
Actual primary completion date
2017-19-06
Actual study completion date
2017-19-06
Plain language summaries
Summary of results in plain language
Available language(s): Dutch, English
To view plain language summaries on trialsummaries.com click here.
Additional information about the trial
Additional information
Not applicable
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