ID
32970
Description
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.
Mots-clés
Versions (3)
- 14/11/2018 14/11/2018 -
- 22/11/2018 22/11/2018 -
- 23/11/2018 23/11/2018 - Sarah Riepenhausen
Détendeur de droits
GlaxoSmithKline
Téléchargé le
22 novembre 2018
DOI
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Licence
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
Description
12-Lead Electrocardiogram
Alias
- UMLS CUI-1
- C0430456 (Electrocardiography, 12-Lead)
- SNOMED
- 268400002
Description
Note: For screening there are only three rows. For sessions there are all of the five rows.
Type de données
integer
Alias
- UMLS CUI [1]
- C0237753 (Numbers)
- SNOMED
- 260299005
- LOINC
- LP6841-3
Description
Date of ECG
Type de données
date
Alias
- UMLS CUI [1]
- C2826640 (Electrocardiogram Date)
Description
Time relative to dosing. Measurement is mandatory for each. Note: the 12hrs and pre dose relative time are only for session 2-6.
Type de données
text
Alias
- UMLS CUI [1]
- C0439564 (Relative time)
- SNOMED
- 118578006
- LOINC
- LP21276-8
Description
00:00-23:59
Type de données
time
Alias
- UMLS CUI [1]
- C0040223 (Time)
- SNOMED
- 410670007
- LOINC
- LP73517-2
Description
Ventricular rate
Type de données
integer
Unités de mesure
- beats / min
Alias
- UMLS CUI [1]
- C2189285 (electrocardiogram: ventricular rate)
Description
PR interval
Type de données
integer
Unités de mesure
- msec
Alias
- UMLS CUI [1]
- C0429087 (Electrocardiogram: P-R interval)
- SNOMED
- 365411005
Description
QRS duration
Type de données
integer
Unités de mesure
- msec
Alias
- UMLS CUI [1]
- C0429025 (QRS complex duration (observable entity))
- SNOMED
- 251208001
- LOINC
- LP31031-5
Description
QT interval
Type de données
integer
Unités de mesure
- msec
Alias
- UMLS CUI [1]
- C0577807 (QT interval duration)
- SNOMED
- 301117000
Description
QTc interval
Type de données
integer
Unités de mesure
- msec
Alias
- UMLS CUI [1]
- C0489625 (QTC interval)
- LOINC
- LP31071-1
Description
ECG normal
Type de données
boolean
Alias
- UMLS CUI [1]
- C0522054 (ECG normal)
- SNOMED
- 164854000
Description
ECG Abnormalities present
Type de données
boolean
Alias
- UMLS CUI [1]
- C0522055 (Electrocardiogram abnormal (finding))
- SNOMED
- 102594003
- LOINC
- LA24621-7
Description
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.
Type de données
text
Alias
- UMLS CUI [1,1]
- C1704258 (Abnormality)
- UMLS CUI [1,2]
- C2985739 (Clinically Significant Indicator)
Similar models
Electrocardiogram
- StudyEvent: ODM
C2985739 (UMLS CUI [1,2])
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