0 Evaluaciones
ID

27194

Descripción

Study ID: 101468/188 Clinical Study ID: SKF-101468/188 Study Title:A Study of the Maintained Efficacy and Safety of Ropinirole Versus Placebo in the Long Term Treatment of Restless Legs Syndrome (RLS) Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 3 Study Recruitment Status: Completed Generic Name: ropinirole Trade Name: Requip Study Indication: Parkinson Disease Module: Screening

Palabras clave

Versiones (1)
  1. 3/11/17 3/11/17 -
Titular de derechos de autor

GlaxoSmithKline

Subido en

3 de noviembre de 2017

DOI

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Licencia

Creative Commons BY-NC 3.0
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    GSK Ropinirole in Patients Suffering from Restless Legs Syndrome 101468/188

    Inglés

    Screening

    1 formularios  
    1. StudyEvent: ODM
      1. Screening
    Concomitant Medication
    Descripción

    Concomitant Medication

    Alias
    UMLS CUI-1
    C2347852
    UMLS CUI-2
    C0035258
    Drug Name (Trade Name Preferred) Concomitant Medication
    Descripción

    Drug Name Concomitant Medication

    Tipo de datos

    text

    Alias
    UMLS CUI [1,1]
    C2360065
    UMLS CUI [1,2]
    C2347852
    Total Daily Dose (e.g 500 mg) Concomitant Medication
    Descripción

    Total Daily Dose Concomitant Medication

    Tipo de datos

    float

    Unidades de medida
    • mg
    Alias
    UMLS CUI [1,1]
    C2348070
    UMLS CUI [1,2]
    C2347852
    mg
    Medical Illness / Diagnosis (or symptom in absence of diagnosis) Concomitant Medication
    Descripción

    Medical Illness / Diagnosis Concomitant Medication

    Tipo de datos

    text

    Alias
    UMLS CUI [1,1]
    C0011900
    UMLS CUI [1,2]
    C2347852
    UMLS CUI [1,3]
    C3146298
    Start Date Concomitant Medication (be as precise as possible)
    Descripción

    Start Date Concomitant Medication

    Tipo de datos

    date

    Alias
    UMLS CUI [1,1]
    C0808070
    UMLS CUI [1,2]
    C2347852
    End Date Concomitant Medication
    Descripción

    End Date Concomitant Medication

    Tipo de datos

    date

    Alias
    UMLS CUI [1,1]
    C0806020
    UMLS CUI [1,2]
    C2347852
    Continuing Concomitant Medication
    Descripción

    Continuing Concomitant Medication

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C2826666
    Volver a la parte superior de la página

    Similar models

    Screening

    1 formularios
    1. StudyEvent: ODM
      1. Screening
    Name
    Tipo
    Description | Question | Decode (Coded Value)
    Tipo de datos
    Alias
    Item Group
    Concomitant Medication
    C2347852 (UMLS CUI-1)
    C0035258 (UMLS CUI-2)
    Drug Name Concomitant Medication
    Item
    Drug Name (Trade Name Preferred) Concomitant Medication
    text
    C2360065 (UMLS CUI [1,1])
    C2347852 (UMLS CUI [1,2])
    Total Daily Dose Concomitant Medication
    Item
    Total Daily Dose (e.g 500 mg) Concomitant Medication
    float
    C2348070 (UMLS CUI [1,1])
    C2347852 (UMLS CUI [1,2])
    Medical Illness / Diagnosis Concomitant Medication
    Item
    Medical Illness / Diagnosis (or symptom in absence of diagnosis) Concomitant Medication
    text
    C0011900 (UMLS CUI [1,1])
    C2347852 (UMLS CUI [1,2])
    C3146298 (UMLS CUI [1,3])
    Start Date Concomitant Medication
    Item
    Start Date Concomitant Medication (be as precise as possible)
    date
    C0808070 (UMLS CUI [1,1])
    C2347852 (UMLS CUI [1,2])
    End Date Concomitant Medication
    Item
    End Date Concomitant Medication
    date
    C0806020 (UMLS CUI [1,1])
    C2347852 (UMLS CUI [1,2])
    Continuing Concomitant Medication
    Item
    Continuing Concomitant Medication
    boolean
    C2826666 (UMLS CUI [1])
    Volver a la parte superior de la página 

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