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临床试验/NCT02982187
NCT02982187已完成4 期

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)

GlaxoSmithKline6 个研究点 分布在 2 个国家目标入组 160 人开始时间: 2016年12月30日最近更新:
适应症
干预措施

试验速览

阶段
4 期
状态
已完成
入组人数
160
试验地点
6
主要终点
Percentage of Participants Making at Least One Critical Error After Reading the Patient Information Leaflets (PIL)

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
None

入排标准

年龄范围
40 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Sub-study 1 : ELLIPTA followed by DISKUS+ HANDIHALER +PQ1

Experimental

In this sequence, subjects will be randomized to use ELLIPTA inhaler in period 1 and then DISKUS + HANDIHALER in period 2. At the end of Visit 1, subjects will complete version 1 of the PQ (PQ1)

干预措施: Placebo ELLIPTA (Device)

Sub-study 1 : ELLIPTA followed by DISKUS+ HANDIHALER +PQ1

Experimental

In this sequence, subjects will be randomized to use ELLIPTA inhaler in period 1 and then DISKUS + HANDIHALER in period 2. At the end of Visit 1, subjects will complete version 1 of the PQ (PQ1)

干预措施: Placebo DISKUS (Device)

Sub-study 1 : ELLIPTA followed by DISKUS+ HANDIHALER +PQ1

Experimental

In this sequence, subjects will be randomized to use ELLIPTA inhaler in period 1 and then DISKUS + HANDIHALER in period 2. At the end of Visit 1, subjects will complete version 1 of the PQ (PQ1)

干预措施: Placebo HANDIHALER (Device)

Sub-study 1 : DISKUS + HANDIHALER followed by ELLIPTA+PQ2

Experimental

In this sequence, subjects will be randomized to use DISKUS + HANDIHALER in period 1 and then ELLIPTA in period 2. At the end of Visit 1, subjects will complete version 2 of the PQ (PQ2)

干预措施: Placebo ELLIPTA (Device)

Sub-study 1 : DISKUS + HANDIHALER followed by ELLIPTA+PQ2

Experimental

In this sequence, subjects will be randomized to use DISKUS + HANDIHALER in period 1 and then ELLIPTA in period 2. At the end of Visit 1, subjects will complete version 2 of the PQ (PQ2)

干预措施: Placebo DISKUS (Device)

Sub-study 1 : DISKUS + HANDIHALER followed by ELLIPTA+PQ2

Experimental

In this sequence, subjects will be randomized to use DISKUS + HANDIHALER in period 1 and then ELLIPTA in period 2. At the end of Visit 1, subjects will complete version 2 of the PQ (PQ2)

干预措施: Placebo HANDIHALER (Device)

Sub-study 1 : DISKUS + HANDIHALER followed by ELLIPTA+PQ2

Experimental

In this sequence, subjects will be randomized to use DISKUS + HANDIHALER in period 1 and then ELLIPTA in period 2. At the end of Visit 1, subjects will complete version 2 of the PQ (PQ2)

干预措施: PQ2 (Other)

Sub-study 1 : ELLIPTA followed by DISKUS+ HANDIHALER +PQ2

Experimental

In this sequence, subjects will be randomized to use ELLIPTA inhaler in period 1 and then DISKUS + HANDIHALER in period 2. At the end of Visit 1, subjects will complete PQ2

干预措施: Placebo ELLIPTA (Device)

Sub-study 1 : ELLIPTA followed by DISKUS+ HANDIHALER +PQ2

Experimental

In this sequence, subjects will be randomized to use ELLIPTA inhaler in period 1 and then DISKUS + HANDIHALER in period 2. At the end of Visit 1, subjects will complete PQ2

干预措施: Placebo DISKUS (Device)

Sub-study 1 : ELLIPTA followed by DISKUS+ HANDIHALER +PQ2

Experimental

In this sequence, subjects will be randomized to use ELLIPTA inhaler in period 1 and then DISKUS + HANDIHALER in period 2. At the end of Visit 1, subjects will complete PQ2

干预措施: Placebo HANDIHALER (Device)

Sub-study 1 : ELLIPTA followed by DISKUS+ HANDIHALER +PQ2

Experimental

In this sequence, subjects will be randomized to use ELLIPTA inhaler in period 1 and then DISKUS + HANDIHALER in period 2. At the end of Visit 1, subjects will complete PQ2

干预措施: PQ2 (Other)

Sub-study 1 : DISKUS + HANDIHALER followed by ELLIPTA+PQ1

Experimental

In this sequence, subjects will be randomized to use DISKUS + HANDIHALER in period 1 and then ELLIPTA in period 2. At the end of Visit 1, subjects will complete PQ1

干预措施: Placebo ELLIPTA (Device)

Sub-study 1 : DISKUS + HANDIHALER followed by ELLIPTA+PQ1

Experimental

In this sequence, subjects will be randomized to use DISKUS + HANDIHALER in period 1 and then ELLIPTA in period 2. At the end of Visit 1, subjects will complete PQ1

干预措施: Placebo DISKUS (Device)

Sub-study 1 : DISKUS + HANDIHALER followed by ELLIPTA+PQ1

Experimental

In this sequence, subjects will be randomized to use DISKUS + HANDIHALER in period 1 and then ELLIPTA in period 2. At the end of Visit 1, subjects will complete PQ1

干预措施: Placebo HANDIHALER (Device)

Substudy 2: ELLIPTA followed by TURBUHALER + HANDIHALER +PQ3

Experimental

In this sequence, subjects will be randomized to use ELLIPTA inhaler in period 1 and then TURBUHALER + HANDIHALER in period 2. At the end of Visit 1, subjects will complete version 3 of the PQ (PQ3)

干预措施: Placebo ELLIPTA (Device)

Substudy 2: ELLIPTA followed by TURBUHALER + HANDIHALER +PQ3

Experimental

In this sequence, subjects will be randomized to use ELLIPTA inhaler in period 1 and then TURBUHALER + HANDIHALER in period 2. At the end of Visit 1, subjects will complete version 3 of the PQ (PQ3)

干预措施: Placebo TURBUHALER (Device)

Substudy 2: ELLIPTA followed by TURBUHALER + HANDIHALER +PQ3

Experimental

In this sequence, subjects will be randomized to use ELLIPTA inhaler in period 1 and then TURBUHALER + HANDIHALER in period 2. At the end of Visit 1, subjects will complete version 3 of the PQ (PQ3)

干预措施: Placebo HANDIHALER (Device)

Substudy 2: ELLIPTA followed by TURBUHALER + HANDIHALER +PQ3

Experimental

In this sequence, subjects will be randomized to use ELLIPTA inhaler in period 1 and then TURBUHALER + HANDIHALER in period 2. At the end of Visit 1, subjects will complete version 3 of the PQ (PQ3)

干预措施: PQ3 (Other)

Substudy 2: TURBUHALER + HANDIHALER followed by ELLIPTA+PQ4

Experimental

In this sequence, subjects will be randomized to use TURBUHALER + HANDIHALER inhaler in period 1 and then ELLIPTA in period 2. At the end of Visit 1, subjects will complete version 4 of the PQ (PQ4)

干预措施: Placebo ELLIPTA (Device)

Substudy 2: TURBUHALER + HANDIHALER followed by ELLIPTA+PQ4

Experimental

In this sequence, subjects will be randomized to use TURBUHALER + HANDIHALER inhaler in period 1 and then ELLIPTA in period 2. At the end of Visit 1, subjects will complete version 4 of the PQ (PQ4)

干预措施: Placebo TURBUHALER (Device)

Substudy 2: TURBUHALER + HANDIHALER followed by ELLIPTA+PQ4

Experimental

In this sequence, subjects will be randomized to use TURBUHALER + HANDIHALER inhaler in period 1 and then ELLIPTA in period 2. At the end of Visit 1, subjects will complete version 4 of the PQ (PQ4)

干预措施: Placebo HANDIHALER (Device)

Substudy 2: TURBUHALER + HANDIHALER followed by ELLIPTA+PQ4

Experimental

In this sequence, subjects will be randomized to use TURBUHALER + HANDIHALER inhaler in period 1 and then ELLIPTA in period 2. At the end of Visit 1, subjects will complete version 4 of the PQ (PQ4)

干预措施: PQ4 (Other)

Substudy 2: ELLIPTA followed by TURBUHALER + HANDIHALER +PQ4

Experimental

In this sequence, subjects will be randomized to use ELLIPTA inhaler in period 1 and then TURBUHALER + HANDIHALER in period 2. At the end of Visit 1, subjects will complete PQ4

干预措施: Placebo ELLIPTA (Device)

Substudy 2: ELLIPTA followed by TURBUHALER + HANDIHALER +PQ4

Experimental

In this sequence, subjects will be randomized to use ELLIPTA inhaler in period 1 and then TURBUHALER + HANDIHALER in period 2. At the end of Visit 1, subjects will complete PQ4

干预措施: Placebo TURBUHALER (Device)

Substudy 2: ELLIPTA followed by TURBUHALER + HANDIHALER +PQ4

Experimental

In this sequence, subjects will be randomized to use ELLIPTA inhaler in period 1 and then TURBUHALER + HANDIHALER in period 2. At the end of Visit 1, subjects will complete PQ4

干预措施: Placebo HANDIHALER (Device)

Substudy 2: ELLIPTA followed by TURBUHALER + HANDIHALER +PQ4

Experimental

In this sequence, subjects will be randomized to use ELLIPTA inhaler in period 1 and then TURBUHALER + HANDIHALER in period 2. At the end of Visit 1, subjects will complete PQ4

干预措施: PQ4 (Other)

Substudy 2: TURBUHALER + HANDIHALER followed by ELLIPTA+PQ3

Experimental

In this sequence, subjects will be randomized to use TURBUHALER + HANDIHALER inhaler in period 1 and then ELLIPTA in period 2. At the end of Visit 1, subjects will complete PQ3

干预措施: Placebo ELLIPTA (Device)

Substudy 2: TURBUHALER + HANDIHALER followed by ELLIPTA+PQ3

Experimental

In this sequence, subjects will be randomized to use TURBUHALER + HANDIHALER inhaler in period 1 and then ELLIPTA in period 2. At the end of Visit 1, subjects will complete PQ3

干预措施: Placebo TURBUHALER (Device)

Substudy 2: TURBUHALER + HANDIHALER followed by ELLIPTA+PQ3

Experimental

In this sequence, subjects will be randomized to use TURBUHALER + HANDIHALER inhaler in period 1 and then ELLIPTA in period 2. At the end of Visit 1, subjects will complete PQ3

干预措施: Placebo HANDIHALER (Device)

Substudy 2: TURBUHALER + HANDIHALER followed by ELLIPTA+PQ3

Experimental

In this sequence, subjects will be randomized to use TURBUHALER + HANDIHALER inhaler in period 1 and then ELLIPTA in period 2. At the end of Visit 1, subjects will complete PQ3

干预措施: PQ3 (Other)

Sub-study 1 : DISKUS + HANDIHALER followed by ELLIPTA+PQ1

Experimental

In this sequence, subjects will be randomized to use DISKUS + HANDIHALER in period 1 and then ELLIPTA in period 2. At the end of Visit 1, subjects will complete PQ1

干预措施: PQ1 (Other)

Sub-study 1 : ELLIPTA followed by DISKUS+ HANDIHALER +PQ1

Experimental

In this sequence, subjects will be randomized to use ELLIPTA inhaler in period 1 and then DISKUS + HANDIHALER in period 2. At the end of Visit 1, subjects will complete version 1 of the PQ (PQ1)

干预措施: PQ1 (Other)

结局指标

主要结局

Percentage of Participants Making at Least One Critical Error After Reading the Patient Information Leaflets (PIL)

时间窗: Day 1

Participants were provided with the relevant section of the PIL, explaining correct use, for each DPI they were to be tested on. A critical error was defined as an error that was most likely to result in no, or a significantly reduced amount, of medication being inhaled by the participant. After reading the PIL for each DPI to be tested, participants demonstrated the DPI and critical errors made by the participants while using each DPI were recorded by the Healthcare Professional (HCP) on the checklists provided. Percentage of participants making at least one critical error after reading PIL were reported.

次要结局

  • The Median Time to Demonstrate Correct Inhaler Use (T1+T2)(Day 1)
  • Time Taken to Read the PIL and Demonstrate Correct Inhaler Use (T1)(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)(Day 1)
  • Percentage of Participants Making at Least One Critical Error After the First Instruction From the HCP(Day 1)
  • Percentage of Participants Making at Least One Critical Error After the Second Instruction From the HCP(Day 1)
  • Percentage of Participants Making at Least One Overall Error After Reading the PIL(Day 1)
  • Percentage of Participants Making at Least One Overall Error After the First Instruction From the HCP(Day 1)
  • Percentage of Participants Making at Least One Overall Error After the Second Instruction From the HCP(Day 1)
  • Number of Participants With Instructions (0, 1 or 2 Times) From the HCP Which Are Needed to Demonstrate Correct Inhaler Use(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(Day 1)
  • Number of Participants With Treatment Preference Based on Responses to the Preference Questionnaire, Which Considered Overall Treatment Preference(Day 1)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (6)

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