Errors in the Use of Turbuhaler and Spiromax Devices Patients With Asthma

NCT ID: NCT02983994

Last Updated: 2018-05-23

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

64 participants

Study Classification

OBSERVATIONAL

Study Start Date

2016-11-30

Study Completion Date

2017-10-10

Brief Summary

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The aim of the study is to evaluate the errors that may occur during inhalation of two devices in patients with asthma, as well as to study whether it relates to the degree of control of patient symptoms and the degree of compliance of medication symptoms. Finally, we also want to study the degree of patient satisfaction with each of the inhalers studied

Detailed Description

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Conditions

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Asthma

Study Design

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Observational Model Type

OTHER

Study Time Perspective

PROSPECTIVE

Study Groups

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Patients with asthma with an inhaled steroid

Patients with a diagnosis of asthma with indication of Treatment with an inhaled steroid (CI)

TURBUHALER®

Intervention Type DEVICE

Patients with asthma with an inhaled Beta agonist

Patients with a diagnosis of asthma with indication of Treatment with an inhaled Beta agonist (LABA)

SPIROMAX®

Intervention Type DEVICE

Interventions

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TURBUHALER®

Intervention Type DEVICE

SPIROMAX®

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Diagnosis of asthma with treatment indication with CI + LABA according to GINA 2015 guide and in dry powder device.
* Over 18 years.
* Patient in stable phase without having had exacerbations in the 3 months previous to the Inclusion in the study

Exclusion Criteria

* Presence of relevant respiratory disease other than asthma (including COPD).
* Refusal to participate in the study and sign informed consent or inability to To give informed consent.
* Patients who have previously been treated with inhaled dust devices dry.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Fundación Pública Andaluza Progreso y Salud

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Hospital Universitario Puerta del Mar

Cadiz, , Spain

Site Status

Hospital Regional de Málaga

Málaga, , Spain

Site Status

Hospital Universitario Virgen Macarena

Seville, , Spain

Site Status

Hospital Universitario Virgen del Rocío

Seville, , Spain

Site Status

Countries

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Spain

Other Identifiers

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FPS-INH-2016-01

Identifier Type: -

Identifier Source: org_study_id

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