ID
32831
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 alcohol urine test and drug screen form. Their have to be filled in for period 1, 2, 3, 4 and 5 and for screening.
Palabras clave
Versiones (4)
- 13/11/18 13/11/18 -
- 16/11/18 16/11/18 -
- 22/11/18 22/11/18 -
- 22/11/18 22/11/18 -
Titular de derechos de autor
GlaxoSmithKline
Subido en
16 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
Alcohol urine test, Drug screen.
- StudyEvent: ODM
Descripción
Alcohol Urine Test
Alias
- UMLS CUI-1
- C0202304
- UMLS CUI-2
- C0042036
Descripción
Date sample taken
Tipo de datos
date
Alias
- UMLS CUI [1]
- C1302413
Descripción
If it's positive, EXCLUDE subject from the study
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0202304
- UMLS CUI [1,2]
- C0042036
Descripción
Note the Initials
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0202304
- UMLS CUI [1,2]
- C0008961
- UMLS CUI [1,3]
- C2986440
Descripción
Drugs of Abuse Screen
Alias
- UMLS CUI-1
- C0038577
Descripción
Date of sample
Tipo de datos
date
Alias
- UMLS CUI [1]
- C1302413
Descripción
If positive, EXCLUDE subject from the study.
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0376196
Descripción
If positive, EXCLUDE subject from the study.
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0009170
Descripción
If positive, EXCLUDE subject from the study.
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0004745
Descripción
If positive, EXCLUDE subject from the study.
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0002667
Descripción
If positive, EXCLUDE subject from the study.
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0005064
Descripción
If positive, EXCLUDE subject from the study.
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0936079
Similar models
Alcohol urine test, Drug screen.
- StudyEvent: ODM
C1948053 (UMLS CUI [1,2])
C0008961 (UMLS CUI [1,2])
C2986440 (UMLS CUI [1,3])