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OpenTrials
Completed

NCT Number: NCT06346678

Accuracy of Accuhaler Tester, Ellipta Tester and Turbutester in Patients With Chronic Obstructive Pulmonary Disease

The goal of this observational study is to investigate the accuracy of Accuhaler tester, Ellipta tester and Turbutester in patients with chronic obstructive pulmonary disease (COPD). The main question it aims to answer is:

• Do Accuhaler tester, Ellipta tester, and Turbutester demonstrate comparable accuracy to the In-check DIAL for assessing inspiratory inhalation force in COPD patients?

Completed

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Key information

Age range

40 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Narongkorn Saiphoklang

Pathum Thani, Changwat Pathum Thani, 12120, Thailand

About this study

This study is a cross-sectional study. COPD patients aged 40 years or older will be included. Peak inspiratory flow rate (PIFR) will be assessed using In-check DIAL as the standard tool. PIFR will be tested in each patient using Accuhaler tester, Ellipta tester and Turbutester.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • COPD diagnosis with confirmed by post-bronchodilator forced expiratory volume in 1 second (FEV1)/forced vital capacity (FVC) <0.7
  • Age 40 years or older
  • Smoking history 10 pack-years or more

Exclusion criteria

  • COPD exacerbation within 3 months
  • Oral or intravenous corticosteroid treatment within 6 weeks
  • Inability to perform assessment of peak inspiratory flow rate
  • Asthma
  • Tracheostomy, invasive or noninvasive mechanical ventilation

Treatment and study plan

Accuhaler tester

Other

Patients will perform testing with Accuhaler tester, Ellipta tester and Turbutester.

Other names: Ellipta tester, Turbutester

Primary outcomes

  1. Accuracy of Accuhaler tester

    Time frame: At day 1 of the study

    Percentage

  2. Accuracy of Ellipta tester

    Time frame: At day 1 of the study

    Percentage

  3. Accuracy of Turbutester

    Time frame: At day 1 of the study

    Percentage

Secondary outcomes

  1. Prevalence of suboptimal peak inspiratory flow rate

    Time frame: At day 1 of the study

    Percentage

  2. Prevalence of insufficient peak inspiratory flow rate

    Time frame: At day 1 of the study

    Percentage

Sponsors and collaborators

Lead sponsor

Thammasat University

Other

Registry information

Important dates

Study start
2024
Primary completion
2024
Study completion
2024
First posted
Apr 4, 2024
Registry last updated
Feb 2, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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