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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.

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Versions (3)
  1. 14/11/2018 14/11/2018 -
  2. 22/11/2018 22/11/2018 -
  3. 23/11/2018 23/11/2018 - Sarah Riepenhausen
Détendeur de droits

GlaxoSmithKline

Téléchargé le

22 novembre 2018

DOI

Pour une demande vous connecter.

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

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    Electrocardiogram

    1 Formulaires  
    1. StudyEvent: ODM
      1. Electrocardiogram
    Administrative data
    Description

    Administrative data

    Alias
    UMLS CUI-1
    C1320722
    Subject number
    Description

    Subject number

    Type de données

    text

    Alias
    UMLS CUI [1]
    C2348585
    Session Number
    Description

    Session Number

    Type de données

    integer

    Alias
    UMLS CUI [1,1]
    C1883017
    UMLS CUI [1,2]
    C0750480
    12-Lead Electrocardiogram
    Description

    12-Lead Electrocardiogram

    Alias
    UMLS CUI-1
    C0430456
    Row no.
    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
    Date of ECG
    Description

    Date of ECG

    Type de données

    date

    Alias
    UMLS CUI [1]
    C2826640
    Planned relative time
    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
    Actual time
    Description

    00:00-23:59

    Type de données

    time

    Alias
    UMLS CUI [1]
    C0040223
    Ventricular rate
    Description

    Ventricular rate

    Type de données

    integer

    Unités de mesure
    • beats / min
    Alias
    UMLS CUI [1]
    C2189285
    beats / min
    PR interval
    Description

    PR interval

    Type de données

    integer

    Unités de mesure
    • msec
    Alias
    UMLS CUI [1]
    C0429087
    msec
    QRS duration
    Description

    QRS duration

    Type de données

    integer

    Unités de mesure
    • msec
    Alias
    UMLS CUI [1]
    C0429025
    msec
    QT interval
    Description

    QT interval

    Type de données

    integer

    Unités de mesure
    • msec
    Alias
    UMLS CUI [1]
    C0577807
    msec
    QTc interval
    Description

    QTc interval

    Type de données

    integer

    Unités de mesure
    • msec
    Alias
    UMLS CUI [1]
    C0489625
    msec
    ECG normal
    Description

    ECG normal

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0522054
    ECG Abnormalities present
    Description

    ECG Abnormalities present

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0522055
    If abnormalities, is the abnormality clinically significant?
    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
    UMLS CUI [1,2]
    C2985739
    Retour au début de la page

    Similar models

    Electrocardiogram

    1 Formulaires
    1. StudyEvent: ODM
      1. Electrocardiogram
    Name
    Type
    Description | Question | Decode (Coded Value)
    Type de données
    Alias
    Item Group
    Administrative data
    C1320722 (UMLS CUI-1)
    Subject number
    Item
    Subject number
    text
    C2348585 (UMLS CUI [1])
    Item
    Session Number
    integer
    C1883017 (UMLS CUI [1,1])
    C0750480 (UMLS CUI [1,2])
    Session Number
    Code List
    Session Number
    CL Item
    1 (1)
    CL Item
    2 (2)
    CL Item
    3 (3)
    CL Item
    4 (4)
    CL Item
    5 (5)
    CL Item
    6 (6)
    Item Group
    12-Lead Electrocardiogram
    C0430456 (UMLS CUI-1)
    Item
    Row no.
    integer
    C0237753 (UMLS CUI [1])
    Row no.
    Code List
    Row no.
    CL Item
    1 (1)
    CL Item
    2 (2)
    CL Item
    3 (3)
    CL Item
    4 (4)
    CL Item
    5 (5)
    Date of ECG
    Item
    Date of ECG
    date
    C2826640 (UMLS CUI [1])
    Item
    Planned relative time
    text
    C0439564 (UMLS CUI [1])
    Planned relative time
    Code List
    Planned relative time
    CL Item
    Screening (S)
    CL Item
    Pre dose (P)
    CL Item
    12hrs (Hrs)
    CL Item
    Unscheduled (U)
    Actual time
    Item
    Actual time
    time
    C0040223 (UMLS CUI [1])
    Ventricular rate
    Item
    Ventricular rate
    integer
    C2189285 (UMLS CUI [1])
    PR interval
    Item
    PR interval
    integer
    C0429087 (UMLS CUI [1])
    QRS duration
    Item
    QRS duration
    integer
    C0429025 (UMLS CUI [1])
    QT interval
    Item
    QT interval
    integer
    C0577807 (UMLS CUI [1])
    QTc interval
    Item
    QTc interval
    integer
    C0489625 (UMLS CUI [1])
    ECG normal
    Item
    ECG normal
    boolean
    C0522054 (UMLS CUI [1])
    ECG Abnormalities present
    Item
    ECG Abnormalities present
    boolean
    C0522055 (UMLS CUI [1])
    Item
    If abnormalities, is the abnormality clinically significant?
    text
    C1704258 (UMLS CUI [1,1])
    C2985739 (UMLS CUI [1,2])
    Abnormality clinically significant
    Code List
    If abnormalities, is the abnormality clinically significant?
    CL Item
    Yes (Y)
    CL Item
    No (N)
    Retour au début de la page 

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