ID
33004
Beskrivning
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 vital signs form. It has to be filled in at screnning, for session 2, 3,4, 5 and 6.
Nyckelord
Versioner (3)
- 2018-11-14 2018-11-14 -
- 2018-11-22 2018-11-22 -
- 2018-11-23 2018-11-23 - Sarah Riepenhausen
Rättsinnehavare
GlaxoSmithKline
Uppladdad den
23 november 2018
DOI
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Licens
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
Vital signs
- StudyEvent: ODM
Beskrivning
Vital Signs
Alias
- UMLS CUI-1
- C0518766 (Vital signs)
- LOINC
- LP30605-7
Beskrivning
Row no.
Datatyp
integer
Alias
- UMLS CUI [1]
- C0237753 (Numbers)
- SNOMED
- 260299005
- LOINC
- LP6841-3
Beskrivning
Date of vital signs
Datatyp
date
Alias
- UMLS CUI [1,1]
- C0011008 (Date in time)
- SNOMED
- 410671006
- UMLS CUI [1,2]
- C0518766 (Vital signs)
- LOINC
- LP30605-7
Beskrivning
Time relative to dosing. Please fill out at least one measurement for screening and one pre-dose measurement for each treatment period. For all additional measurements choose "unscheduled".
Datatyp
text
Alias
- UMLS CUI [1]
- C0439564 (Relative time)
- SNOMED
- 118578006
- LOINC
- LP21276-8
Beskrivning
00:00-23:59
Datatyp
time
Alias
- UMLS CUI [1]
- C0040223 (Time)
- SNOMED
- 410670007
- LOINC
- LP73517-2
Beskrivning
NOTE: HR and BP measurements will be made with the subject in a supine position having rested in this position for at least 10 minutes before each reading.
Datatyp
integer
Måttenheter
- mmHg
Alias
- UMLS CUI [1]
- C0871470 (Systolic Pressure)
- SNOMED
- 271649006
Beskrivning
NOTE: HR and BP measurements will be made with the subject in a supine position having rested in this position for at least 10 minutes before each reading.
Datatyp
integer
Måttenheter
- mmHg
Alias
- UMLS CUI [1]
- C0428883 (Diastolic blood pressure)
- SNOMED
- 271650006
Beskrivning
NOTE: HR and BP measurements will be made with the subject in a supine position having rested in this position for at least 10 minutes before each reading.
Datatyp
integer
Måttenheter
- beats / min
Alias
- UMLS CUI [1]
- C0018810 (heart rate)
- SNOMED
- 364075005
- LOINC
- LP29713-2
Beskrivning
Only for session 2-6.
Datatyp
integer
Måttenheter
- °C
Alias
- UMLS CUI [1]
- C0005903 (Body Temperature)
- SNOMED
- 722490005
- LOINC
- LP36617-6
Similar models
Vital signs
- StudyEvent: ODM
C0518766 (UMLS CUI [1,2])
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