0 Evaluaciones
ID

38554

Descripción

Study ID: 110948 Clinical Study ID: 110948 Study Title: Assessment of the effect of sumatriptan and naproxen sodium combination tablet, sumatriptan tablet, and naproxen sodium tablet treatment on blood pressure when administered intermittently for six months for the acute treatment of migraine attacks, with or without aura, in adults Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00792636 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 4 Study Recruitment Status: Completed Generic Name: sumatriptan and naproxen sodium combination tablet Trade Name: sumatriptan tablet, naproxen sodium tablet Study Indication: Migraine Disorders

Palabras clave

Versiones (2)
  1. 9/10/19 9/10/19 -
  2. 24/10/19 24/10/19 -
Titular de derechos de autor

GlaxoSmithKline

Subido en

24 de octubre de 2019

DOI

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Licencia

Creative Commons BY-NC 3.0
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    Sumatriptan and Naproxen Sodium for Acute Treatment of Migraine Attacks; NCT00792636

    Inglés

    Common CRF : Meds Recorded at Home

    1 formularios  
    Administrative Data
    Descripción

    Administrative Data

    Alias
    UMLS CUI-1
    C1320722
    Site
    Descripción

    Study Site

    Tipo de datos

    text

    Alias
    UMLS CUI [1]
    C2825164
    Patient
    Descripción

    Patient name

    Tipo de datos

    text

    Alias
    UMLS CUI [1]
    C1299487
    Patient No
    Descripción

    Patients, Identification number

    Tipo de datos

    integer

    Alias
    UMLS CUI [1,1]
    C0030705
    UMLS CUI [1,2]
    C1300638
    Meds Recorded at Home
    Descripción

    Meds Recorded at Home

    Alias
    UMLS CUI-1
    C2347852
    UMLS CUI-2
    C0442519
    Sequence Number
    Descripción

    Concomitant Agent, Home environment, Sequence Number

    Tipo de datos

    integer

    Alias
    UMLS CUI [1,1]
    C2347852
    UMLS CUI [1,2]
    C0442519
    UMLS CUI [1,3]
    C2348184
    Drug Name (Trade Name preferred)
    Descripción

    Concomitant Agent, Home environment, Medication name

    Tipo de datos

    text

    Alias
    UMLS CUI [1,1]
    C2347852
    UMLS CUI [1,2]
    C0442519
    UMLS CUI [1,3]
    C2360065
    Modified reported term
    Descripción

    Concomitant Agent, Home environment, Medication name, Reported Term

    Tipo de datos

    text

    Alias
    UMLS CUI [1,1]
    C2347852
    UMLS CUI [1,2]
    C0442519
    UMLS CUI [1,3]
    C2360065
    UMLS CUI [1,4]
    C2826302
    GSK Drug synonym
    Descripción

    Concomitant Agent, Home environment, Pharmaceutical Preparations, Synonym

    Tipo de datos

    text

    Alias
    UMLS CUI [1,1]
    C2347852
    UMLS CUI [1,2]
    C0442519
    UMLS CUI [1,3]
    C0013227
    UMLS CUI [1,4]
    C0871468
    GSK Drug Collection code
    Descripción

    Concomitant Agent, Home environment, Code

    Tipo de datos

    text

    Alias
    UMLS CUI [1,1]
    C2347852
    UMLS CUI [1,2]
    C0442519
    UMLS CUI [1,3]
    C0805701
    Failed coding
    Descripción

    Concomitant Agent, Home environment, Code, Failed

    Tipo de datos

    text

    Alias
    UMLS CUI [1,1]
    C2347852
    UMLS CUI [1,2]
    C0442519
    UMLS CUI [1,3]
    C0805701
    UMLS CUI [1,4]
    C0231175
    Date Taken
    Descripción

    Concomitant Agent, Home environment, Date in time

    Tipo de datos

    date

    Alias
    UMLS CUI [1,1]
    C2347852
    UMLS CUI [1,2]
    C0442519
    UMLS CUI [1,3]
    C0011008
    Time Taken
    Descripción

    Concomitant Agent, Home environment, Time

    Tipo de datos

    time

    Alias
    UMLS CUI [1,1]
    C2347852
    UMLS CUI [1,2]
    C0442519
    UMLS CUI [1,3]
    C0040223
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    Similar models

    Common CRF : Meds Recorded at Home

    1 formularios
    Name
    Tipo
    Description | Question | Decode (Coded Value)
    Tipo de datos
    Alias
    Item Group
    Administrative Data
    C1320722 (UMLS CUI-1)
    Study Site
    Item
    Site
    text
    C2825164 (UMLS CUI [1])
    Patient name
    Item
    Patient
    text
    C1299487 (UMLS CUI [1])
    Patients, Identification number
    Item
    Patient No
    integer
    C0030705 (UMLS CUI [1,1])
    C1300638 (UMLS CUI [1,2])
    Item Group
    Meds Recorded at Home
    C2347852 (UMLS CUI-1)
    C0442519 (UMLS CUI-2)
    Concomitant Agent, Home environment, Sequence Number
    Item
    Sequence Number
    integer
    C2347852 (UMLS CUI [1,1])
    C0442519 (UMLS CUI [1,2])
    C2348184 (UMLS CUI [1,3])
    Concomitant Agent, Home environment, Medication name
    Item
    Drug Name (Trade Name preferred)
    text
    C2347852 (UMLS CUI [1,1])
    C0442519 (UMLS CUI [1,2])
    C2360065 (UMLS CUI [1,3])
    Concomitant Agent, Home environment, Medication name, Reported Term
    Item
    Modified reported term
    text
    C2347852 (UMLS CUI [1,1])
    C0442519 (UMLS CUI [1,2])
    C2360065 (UMLS CUI [1,3])
    C2826302 (UMLS CUI [1,4])
    Concomitant Agent, Home environment, Pharmaceutical Preparations, Synonym
    Item
    GSK Drug synonym
    text
    C2347852 (UMLS CUI [1,1])
    C0442519 (UMLS CUI [1,2])
    C0013227 (UMLS CUI [1,3])
    C0871468 (UMLS CUI [1,4])
    Concomitant Agent, Home environment, Code
    Item
    GSK Drug Collection code
    text
    C2347852 (UMLS CUI [1,1])
    C0442519 (UMLS CUI [1,2])
    C0805701 (UMLS CUI [1,3])
    Concomitant Agent, Home environment, Code, Failed
    Item
    Failed coding
    text
    C2347852 (UMLS CUI [1,1])
    C0442519 (UMLS CUI [1,2])
    C0805701 (UMLS CUI [1,3])
    C0231175 (UMLS CUI [1,4])
    Concomitant Agent, Home environment, Date in time
    Item
    Date Taken
    date
    C2347852 (UMLS CUI [1,1])
    C0442519 (UMLS CUI [1,2])
    C0011008 (UMLS CUI [1,3])
    Concomitant Agent, Home environment, Time
    Item
    Time Taken
    time
    C2347852 (UMLS CUI [1,1])
    C0442519 (UMLS CUI [1,2])
    C0040223 (UMLS CUI [1,3])
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