Errors in the Use of Turbuhaler and Spiromax Devices Patients With Asthma
NCT ID: NCT02983994
Last Updated: 2018-05-23
Study Results
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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COMPLETED
64 participants
OBSERVATIONAL
2016-11-30
2017-10-10
Brief Summary
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Detailed Description
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Conditions
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Study Design
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OTHER
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®
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®
Interventions
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TURBUHALER®
SPIROMAX®
Eligibility Criteria
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Inclusion Criteria
* Over 18 years.
* Patient in stable phase without having had exacerbations in the 3 months previous to the Inclusion in the study
Exclusion Criteria
* 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.
18 Years
ALL
No
Sponsors
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Fundación Pública Andaluza Progreso y Salud
OTHER
Responsible Party
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Locations
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Hospital Universitario Puerta del Mar
Cadiz, , Spain
Hospital Regional de Málaga
Málaga, , Spain
Hospital Universitario Virgen Macarena
Seville, , Spain
Hospital Universitario Virgen del Rocío
Seville, , Spain
Countries
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Other Identifiers
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FPS-INH-2016-01
Identifier Type: -
Identifier Source: org_study_id
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