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Comparative Study on Usability of Inhaler Devices in Adults With Asthma or COPD - Trial NCT02757209

Access comprehensive clinical trial information for NCT02757209 through Pure Global AI's free database. This phase not specified trial is sponsored by Consorzio Futuro in Ricerca and is currently Completed. The study focuses on Asthma,COPD. Target enrollment is 84 participants.

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NCT02757209
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Trial Details
ClinicalTrials.gov โ€ข NCT02757209
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Comparative Study on Usability of Inhaler Devices in Adults With Asthma or COPD
STUDY NUMBER: PMC-101-APT Usability and Adherence of Spiromaxยฎ Inhaler Device, Turbohalerยฎ and Diskusยฎ Inhaler Devices for Fixed Combination of Corticosteroid/Long-acting beta2- Agonist, in Adults With Asthma or COPD

Study Focus

Asthma,COPD

Spiromax (budesonide/formoterol)

Interventional

device

Sponsor & Location

Consorzio Futuro in Ricerca

Cassano delle Murge,Ferrara,Tradate, Italy

Timeline & Enrollment

N/A

Apr 01, 2016

Jan 01, 2018

84 participants

Primary Outcome

Usability of Spiromax , Turbuhaler and Diskus devices

Summary

This is a randomized, multi-center, active-controlled, repeated measures design study in male
 and female patients 60 years of age and older with persistent asthma or COPD.
 
 Study will be conducted in 4 Italian University/Hospital Centers: Ferrara, Parma, Cassano
 delle Murge (Ba), Tradate.
 
 The primary efficacy parameter of the study is inhaler device usability (expressed as total
 number of repeated attempts required to achieve optimal use).

ICD-10 Classifications

Asthma
Asthma, unspecified
Nonallergic asthma
Mixed asthma
Other chronic obstructive pulmonary disease

Data Source

ClinicalTrials.gov

NCT02757209

Device Trial