ID
32970
Beschrijving
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.
Trefwoorden
Versies (3)
- 14-11-18 14-11-18 -
- 22-11-18 22-11-18 -
- 23-11-18 23-11-18 - Sarah Riepenhausen
Houder van rechten
GlaxoSmithKline
Geüploaded op
22 november 2018
DOI
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Licentie
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
Beschrijving
12-Lead Electrocardiogram
Alias
- UMLS CUI-1
- C0430456
Beschrijving
Note: For screening there are only three rows. For sessions there are all of the five rows.
Datatype
integer
Alias
- UMLS CUI [1]
- C0237753
Beschrijving
Date of ECG
Datatype
date
Alias
- UMLS CUI [1]
- C2826640
Beschrijving
Time relative to dosing. Measurement is mandatory for each. Note: the 12hrs and pre dose relative time are only for session 2-6.
Datatype
text
Alias
- UMLS CUI [1]
- C0439564
Beschrijving
00:00-23:59
Datatype
time
Alias
- UMLS CUI [1]
- C0040223
Beschrijving
Ventricular rate
Datatype
integer
Maateenheden
- beats / min
Alias
- UMLS CUI [1]
- C2189285
Beschrijving
PR interval
Datatype
integer
Maateenheden
- msec
Alias
- UMLS CUI [1]
- C0429087
Beschrijving
QRS duration
Datatype
integer
Maateenheden
- msec
Alias
- UMLS CUI [1]
- C0429025
Beschrijving
QT interval
Datatype
integer
Maateenheden
- msec
Alias
- UMLS CUI [1]
- C0577807
Beschrijving
QTc interval
Datatype
integer
Maateenheden
- msec
Alias
- UMLS CUI [1]
- C0489625
Beschrijving
ECG normal
Datatype
boolean
Alias
- UMLS CUI [1]
- C0522054
Beschrijving
ECG Abnormalities present
Datatype
boolean
Alias
- UMLS CUI [1]
- C0522055
Beschrijving
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.
Datatype
text
Alias
- UMLS CUI [1,1]
- C1704258
- UMLS CUI [1,2]
- C2985739
Similar models
Electrocardiogram
- StudyEvent: ODM
C2985739 (UMLS CUI [1,2])
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