ID
33005
Beschreibung
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 form for Electrocardiogram. It has to be filled in at screening, sessions 2, 3, 4, 5 and 6.
Stichworte
Versionen (3)
- 14.11.18 14.11.18 -
- 22.11.18 22.11.18 -
- 23.11.18 23.11.18 - Sarah Riepenhausen
Rechteinhaber
GlaxoSmithKline
Hochgeladen am
23. November 2018
DOI
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Lizenz
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
Electrocardiogram
- StudyEvent: ODM
Beschreibung
12-Lead Electrocardiogram
Alias
- UMLS CUI-1
- C0430456
Beschreibung
Note: For screening there are only three rows. For sessions there are all of the five rows.
Datentyp
integer
Alias
- UMLS CUI [1]
- C0237753
Beschreibung
Date of ECG
Datentyp
date
Alias
- UMLS CUI [1]
- C2826640
Beschreibung
Time relative to dosing. The 12hrs and pre dose relative time are only for session 2-6, Screening only for session 1. Please choose "unscheduled" in case of additional, unplanned ECGs.
Datentyp
text
Alias
- UMLS CUI [1]
- C0439564
Beschreibung
00:00-23:59
Datentyp
time
Alias
- UMLS CUI [1]
- C0040223
Beschreibung
Ventricular rate
Datentyp
integer
Maßeinheiten
- beats / min
Alias
- UMLS CUI [1]
- C2189285
Beschreibung
PR interval
Datentyp
integer
Maßeinheiten
- msec
Alias
- UMLS CUI [1]
- C0429087
Beschreibung
QRS duration
Datentyp
integer
Maßeinheiten
- msec
Alias
- UMLS CUI [1]
- C0429025
Beschreibung
QT interval
Datentyp
integer
Maßeinheiten
- msec
Alias
- UMLS CUI [1]
- C0577807
Beschreibung
QTc interval
Datentyp
integer
Maßeinheiten
- msec
Alias
- UMLS CUI [1]
- C0489625
Beschreibung
ECG normal
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0522054
Beschreibung
ECG Abnormalities present
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0522055
Beschreibung
If abnormalities are present which are clinically significant, complete additional ECG ABNORMALITIES FORM. Copy the session number from the top of this form and the date and time to the ECG ABNORMALITIES FORM.
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1704258
- UMLS CUI [1,2]
- C2985739
Ähnliche Modelle
Electrocardiogram
- StudyEvent: ODM
C2985739 (UMLS CUI [1,2])
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