ID
32965
Descripción
Study ID: 101877 Clinical Study ID: SAS101877 Study Title: A randomised, open label, 5-way crossover study to assess the systemic exposure of FP and salmeterol from SERETIDE/ADVAIR 250 without spacer, with Aerochamber -Plus and with -Max spacer, with VOLUMATIC spacer and SERETIDE/ADVAIR 500 DISKUS/ACCUHALER in adult subjects with mild or intermittent asthma Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: fluticasone propionate/salmeterol Trade Name: Advair DISKUS,Seretide Accuhaler; Viani,Seretide Diskus,Seretide Accuhaler,Seretide,Advair DISKUS Study Indication: Asthma The study consists of 5 treatment periods and a follow-up visit. The Screening includes Session 1 Treatment Period 1 includes Session 2 Treatment Period 2 includes Session 3 Treatment Period 3 includes Session 4 Treatment Period 4 includes Session 5 Treatment Period 5 includes Session 6 The Follow-up includes Session 7. This document contains the medical history and state of training of subject. It has to be filled in at screening.
Palabras clave
Versiones (3)
- 13/11/18 13/11/18 -
- 16/11/18 16/11/18 -
- 22/11/18 22/11/18 -
Titular de derechos de autor
GlaxoSmithKline
Subido en
22 de noviembre de 2018
DOI
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Licencia
Creative Commons BY-NC 3.0
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Systemic exposure of fluticasone propionate (FP) and salmeterol from different inhalation devices in adults with mild or intermittent asthma, (Study-)ID: 101877
Medical history and training
- StudyEvent: ODM
Descripción
Medical History
Alias
- UMLS CUI-1
- C0262926
Descripción
Medical history, examinaton
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0012634
Descripción
Medical condition status
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0012634
- UMLS CUI [1,2]
- C0449438
Descripción
Medical condition, present
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0012634
Descripción
Training
Alias
- UMLS CUI-1
- C0015259
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