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sTep dOWn Inhalers in the reAl woRlD

Not Applicable
Completed
Conditions
Chronic Obstructive Pulmonary Disease
Interventions
Drug: Any LABA/LAMA
Registration Number
NCT03527927
Lead Sponsor
Hywel Dda Health Board
Brief Summary

To establish the feasibility of stopping inhaled steroids and switching or maintaining dual bronchodilation in one visit - in the real world, for people with COPD.

Detailed Description

COPD patients prescribed a combination of any inhaled corticosteroid (ICS), long acting beta agonist (LABA) and long acting muscarinic antagonist (LAMA) will be switched to a single LABA/LAMA combination inhaler, stopping their ICS. They will be followed up for 12 months.

Participants are shown the four currently available LABA/LAMA combination inhalers and instructed on their use. The clinical specialist will use standard prompts in an effort to demonstrate the inhalers in an unbiased way. The participants will choose: Ultibro® (Breezhaler device) or Duaklir® (Genuair device) or Anoro® (Ellipta device) or Spiolto® (Respimat device) and they will be prescribed the inhaler of their choice provided they can demonstrate effective use.

Patients will be reviewed 4, 12, 26 and at 52 weeks after switching with clinical outcomes measured at these points. As this is a real-world open study the patients and GPs are instructed that treatments can be changed at any point as clinically indicated, including restarting an ICS.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
67
Inclusion Criteria
  • GP diagnosis of COPD
  • Post bronchodilator FEV1/FVC ratio <70% with FEV1<80% predicted
  • Current or ex smoker equal or greater than 10 pack years
  • Taking an ICS, LABA & LAMA
Exclusion Criteria
  • Unable or unwilling to sign informed consent
  • Any previous or current diagnosis of asthma
  • Any features of asthma or large variability in symptoms
  • History of atopy
  • Any previous blood eosinophil count >600mm3
  • A moderate or severe exacerbation of COPD (needing systemic glucocorticosteroids or hospital admission for >24 hours) within the last 6 weeks
  • Life expectancy < 1 year

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
LABA/LAMA inhalerAny LABA/LAMAPatients on a combination of inhaled corticosteroid (ICS), long acting beta agonist (LABA) and long acting muscarinic antagonist (LAMA) will be taken off their current ICS/LABA/LAMA combination inhalers and will commence on a single LABA/LAMA inhaler (any LABA/LAMA) of their choice.
Primary Outcome Measures
NameTimeMethod
Numbers maintained on dual bronchodilationAt 12 months

The proportion of patients with stable COPD who can be successfully switched from triple inhaled therapy (ICS+LABA+LAMA in any combination of inhalers) to dual inhaled bronchodilator therapy (LABA+LAMA)

Secondary Outcome Measures
NameTimeMethod
Exacerbations12 months before and 12 months after enrollment

Comparison of the number of moderate and severe exacerbations in those on LABA+LAMA over 52 weeks compared with those continuing triple therapy

Lung functionBaseline, 4 weeks, 12 weeks, 26 weeks, 52 weeks

Trend in FEV1

COPD assessment test (CAT)Over 12 months

Changes in total CAT score (range 0-40), higher score indicates worse outcome) from baseline, at 4 weeks, 12 weeks, 26 weeks and 52 weeks

EQ-5D-3LOver 12 months

General quality of life visual analogue scale from 0-100, 0 indicates worse imaginable health and 100 best imaginable health. Score reported at baseline, 4 weeks, 12 weeks, 26 weeks and 52 weeks

Moderate or severe exacerbations12 months before and 12 months after enrollment

Comparison of the number of moderate and severe exacerbations in those on LABA+LAMA over 52 weeks compared with their previous 52 weeks

Costs12 months before and 12 months after enrollment

Comparison of total inhaler prescription costs

Restarting inhaled steroidsAt 12 months

Proportion of patients requiring restarting ICS (on the discretion of their clinician) at each visit.

Inhaler device choiceAt enrollment

Proportions of patients choosing each LABA+LAMA device and some reasons why

Trial Locations

Locations (1)

Prince Philip Hospital

🇬🇧

Llanelli, Carmarthenshire, United Kingdom

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