0 Evaluaciones

ID

34086

Descripción

Study ID: 106218 Clinical Study ID: TDC106218 Study Title: Study On Bioavailability And Pharmacokinetics Of Various Doses Of Testosterone Administered With And Without Dutasteride  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: testosterone Trade Name: Andropatch,Androderm Study Indication: Hypogonadism, Male

Palabras clave

  1. 23/10/18 23/10/18 -
  2. 14/1/19 14/1/19 -
Titular de derechos de autor

GlaxoSmithKline

Subido en

14 de enero de 2019

DOI

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Licencia

Creative Commons BY-NC 3.0

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    Bioavailability and Pharmacokinetics of Testosterone with/without Dutasteride - 106218

    Part 2 - Treatment Period day -1 - 12-lead ECG (Semi-Supine)

    12-Lead ECG
    Descripción

    12-Lead ECG

    Alias
    UMLS CUI-1
    C0430456 (Electrocardiography, 12-Lead)
    SNOMED
    268400002
    Start Date of ECG
    Descripción

    12 lead ECG, Start Date

    Tipo de datos

    date

    Alias
    UMLS CUI [1,1]
    C0430456 (Electrocardiography, 12-Lead)
    SNOMED
    268400002
    UMLS CUI [1,2]
    C0808070 (Start Date)
    Start Time of ECG
    Descripción

    12 lead ECG, Start Time

    Tipo de datos

    time

    Alias
    UMLS CUI [1,1]
    C0430456 (Electrocardiography, 12-Lead)
    SNOMED
    268400002
    UMLS CUI [1,2]
    C1301880 (Start time)
    SNOMED
    398201009
    LOINC
    LP102339-1
    Ventricular Rate
    Descripción

    Ventricular Rate

    Tipo de datos

    integer

    Unidades de medida
    • bpm
    Alias
    UMLS CUI [1]
    C2189285 (electrocardiogram: ventricular rate)
    bpm
    PR Interval
    Descripción

    PR Interval

    Tipo de datos

    integer

    Unidades de medida
    • msec
    Alias
    UMLS CUI [1]
    C0429087 (Electrocardiogram: P-R interval)
    SNOMED
    365411005
    msec
    QRS Interval
    Descripción

    Mean QRS Duration

    Tipo de datos

    integer

    Unidades de medida
    • msec
    Alias
    UMLS CUI [1]
    C1880451 (Mean QRS Duration)
    msec
    Uncorrected QT Interval
    Descripción

    QT Interval - finding

    Tipo de datos

    integer

    Unidades de medida
    • msec
    Alias
    UMLS CUI [1]
    C1287082 (QT interval - finding)
    SNOMED
    365417009
    msec
    QTc Interval
    Descripción

    QTc Interval

    Tipo de datos

    integer

    Unidades de medida
    • msec
    Alias
    UMLS CUI [1]
    C0489625 (QTC interval)
    LOINC
    LP31071-1
    msec
    Result of the ECG
    Descripción

    12 lead ECG, Result

    Tipo de datos

    integer

    Alias
    UMLS CUI [1,1]
    C0430456 (Electrocardiography, 12-Lead)
    SNOMED
    268400002
    UMLS CUI [1,2]
    C1274040 (Result)
    SNOMED
    394617004

    Similar models

    Part 2 - Treatment Period day -1 - 12-lead ECG (Semi-Supine)

    Name
    Tipo
    Description | Question | Decode (Coded Value)
    Tipo de datos
    Alias
    Item Group
    12-Lead ECG
    C0430456 (UMLS CUI-1)
    12 lead ECG, Start Date
    Item
    Start Date of ECG
    date
    C0430456 (UMLS CUI [1,1])
    C0808070 (UMLS CUI [1,2])
    12 lead ECG, Start Time
    Item
    Start Time of ECG
    time
    C0430456 (UMLS CUI [1,1])
    C1301880 (UMLS CUI [1,2])
    Ventricular Rate
    Item
    Ventricular Rate
    integer
    C2189285 (UMLS CUI [1])
    PR Interval
    Item
    PR Interval
    integer
    C0429087 (UMLS CUI [1])
    Mean QRS Duration
    Item
    QRS Interval
    integer
    C1880451 (UMLS CUI [1])
    QT Interval - finding
    Item
    Uncorrected QT Interval
    integer
    C1287082 (UMLS CUI [1])
    QTc Interval
    Item
    QTc Interval
    integer
    C0489625 (UMLS CUI [1])
    Item
    Result of the ECG
    integer
    C0430456 (UMLS CUI [1,1])
    C1274040 (UMLS CUI [1,2])
    Code List
    Result of the ECG
    CL Item
    Normal (1)
    CL Item
    Abnormal - not clinically significant  (2)
    CL Item
    Abnormal - clinically significant (Complete the Non-Serious Adverse Events (AE) or Serious Adverse Event (SAE) page(s) if clinically significant abnormalities meet the protocol definition for an AE or SAE. Complete the additional ECG Abnormalities page if clinically significant abnormalities are present.) (3)
    CL Item
    No result (not available) (4)

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