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ID

32970

Descrizione

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.

Keywords

  1. 14/11/18 14/11/18 -
  2. 22/11/18 22/11/18 -
  3. 23/11/18 23/11/18 - Sarah Riepenhausen
Titolare del copyright

GlaxoSmithKline

Caricato su

22 novembre 2018

DOI

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Licenza

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

    1. StudyEvent: ODM
      1. Electrocardiogram
    Administrative data
    Descrizione

    Administrative data

    Alias
    UMLS CUI-1
    C1320722 (Administrative documentation)
    SNOMED
    405624007
    Subject number
    Descrizione

    Subject number

    Tipo di dati

    text

    Alias
    UMLS CUI [1]
    C2348585 (Clinical Trial Subject Unique Identifier)
    Session Number
    Descrizione

    Session Number

    Tipo di dati

    integer

    Alias
    UMLS CUI [1,1]
    C1883017 (Session)
    UMLS CUI [1,2]
    C0750480 (Count)
    12-Lead Electrocardiogram
    Descrizione

    12-Lead Electrocardiogram

    Alias
    UMLS CUI-1
    C0430456 (Electrocardiography, 12-Lead)
    SNOMED
    268400002
    Row no.
    Descrizione

    Note: For screening there are only three rows. For sessions there are all of the five rows.

    Tipo di dati

    integer

    Alias
    UMLS CUI [1]
    C0237753 (Numbers)
    SNOMED
    260299005
    LOINC
    LP6841-3
    Date of ECG
    Descrizione

    Date of ECG

    Tipo di dati

    date

    Alias
    UMLS CUI [1]
    C2826640 (Electrocardiogram Date)
    Planned relative time
    Descrizione

    Time relative to dosing. Measurement is mandatory for each. Note: the 12hrs and pre dose relative time are only for session 2-6.

    Tipo di dati

    text

    Alias
    UMLS CUI [1]
    C0439564 (Relative time)
    SNOMED
    118578006
    LOINC
    LP21276-8
    Actual time
    Descrizione

    00:00-23:59

    Tipo di dati

    time

    Alias
    UMLS CUI [1]
    C0040223 (Time)
    SNOMED
    410670007
    LOINC
    LP73517-2
    Ventricular rate
    Descrizione

    Ventricular rate

    Tipo di dati

    integer

    Unità di misura
    • beats / min
    Alias
    UMLS CUI [1]
    C2189285 (electrocardiogram: ventricular rate)
    beats / min
    PR interval
    Descrizione

    PR interval

    Tipo di dati

    integer

    Unità di misura
    • msec
    Alias
    UMLS CUI [1]
    C0429087 (Electrocardiogram: P-R interval)
    SNOMED
    365411005
    msec
    QRS duration
    Descrizione

    QRS duration

    Tipo di dati

    integer

    Unità di misura
    • msec
    Alias
    UMLS CUI [1]
    C0429025 (QRS complex duration (observable entity))
    SNOMED
    251208001
    LOINC
    LP31031-5
    msec
    QT interval
    Descrizione

    QT interval

    Tipo di dati

    integer

    Unità di misura
    • msec
    Alias
    UMLS CUI [1]
    C0577807 (QT interval duration)
    SNOMED
    301117000
    msec
    QTc interval
    Descrizione

    QTc interval

    Tipo di dati

    integer

    Unità di misura
    • msec
    Alias
    UMLS CUI [1]
    C0489625 (QTC interval)
    LOINC
    LP31071-1
    msec
    ECG normal
    Descrizione

    ECG normal

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1]
    C0522054 (ECG normal)
    SNOMED
    164854000
    ECG Abnormalities present
    Descrizione

    ECG Abnormalities present

    Tipo di dati

    boolean

    Alias
    UMLS CUI [1]
    C0522055 (Electrocardiogram abnormal (finding))
    SNOMED
    102594003
    LOINC
    LA24621-7
    If abnormalities, is the abnormality clinically significant?
    Descrizione

    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.

    Tipo di dati

    text

    Alias
    UMLS CUI [1,1]
    C1704258 (Abnormality)
    UMLS CUI [1,2]
    C2985739 (Clinically Significant Indicator)

    Similar models

    Electrocardiogram

    1. StudyEvent: ODM
      1. Electrocardiogram
    Name
    genere
    Description | Question | Decode (Coded Value)
    Tipo di dati
    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])
    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])
    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])
    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])
    Code List
    If abnormalities, is the abnormality clinically significant?
    CL Item
    Yes (Y)
    CL Item
    No (N)

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