ID

40732

Descripción

Study ID: 101468/218 Clinical Study ID: SKF-101468/218 Study Title:A Single-Blind, Randomised, Placebo-Controlled, Parallel-Group, Multicentre, Phase IIa Study to Determine the Pharmacokinetics and Tolerability of Ropinirole in Patients Suffering from Restless Legs Syndrome (RLS) Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Sponsor: GlaxoSmithKline Phase: phase 2 Study Recruitment Status: Completed Generic Name: ropinirole Trade Name: requip Study Indication: Restless Legs Syndrome

Palabras clave

Versiones (1)
  1. 5/5/20 5/5/20 -
Titular de derechos de autor

GlaxoSmithKline

Subido en

5 de mayo de 2020

DOI

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Licencia

Creative Commons BY-NC 4.0
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    Pharmacokinetics and Tolerability of Ropinirole in Patients Suffering from Restless Legs Syndrome 101468/218

    Inglés

    Pregnancy Test

    1 formularios  
    1. StudyEvent: ODM
      1. Pregnancy Test
    Administrative
    Descripción

    Administrative

    Alias
    UMLS CUI-1
    C1320722
    Patient Number
    Descripción

    Patient Number

    Tipo de datos

    text

    Alias
    UMLS CUI [1]
    C2348585
    Centre Number
    Descripción

    Centre Number

    Tipo de datos

    text

    Alias
    UMLS CUI [1,1]
    C0600091
    UMLS CUI [1,2]
    C0019994
    Visit Date
    Descripción

    Visit Date

    Tipo de datos

    date

    Alias
    UMLS CUI [1]
    C1320303
    Pregnancy Test
    Descripción

    Pregnancy Test

    Alias
    UMLS CUI-1
    C0032976
    Was a pregnancy test carried out?
    Descripción

    Was a pregnancy test carried out?

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0032976
    If no pregnancy test was carried out, specify reason
    Descripción

    If no pregnancy test was carried out, specify reason

    Tipo de datos

    text

    Alias
    UMLS CUI [1,1]
    C0032976
    UMLS CUI [1,2]
    C2826287
    Date of pregnancy test
    Descripción

    Date of pregnancy test

    Tipo de datos

    date

    Alias
    UMLS CUI [1,1]
    C0032976
    UMLS CUI [1,2]
    C0011008
    Result of Pregnancy Test
    Descripción

    Result of Pregnancy Test

    Tipo de datos

    integer

    Alias
    UMLS CUI [1]
    C0427777
    Volver a la parte superior de la página

    Similar models

    Pregnancy Test

    1 formularios
    1. StudyEvent: ODM
      1. Pregnancy Test
    Name
    Tipo
    Description | Question | Decode (Coded Value)
    Tipo de datos
    Alias
    Item Group
    Administrative
    C1320722 (UMLS CUI-1)
    Patient Number
    Item
    Patient Number
    text
    C2348585 (UMLS CUI [1])
    Centre Number
    Item
    Centre Number
    text
    C0600091 (UMLS CUI [1,1])
    C0019994 (UMLS CUI [1,2])
    Visit Date
    Item
    Visit Date
    date
    C1320303 (UMLS CUI [1])
    Item Group
    Pregnancy Test
    C0032976 (UMLS CUI-1)
    Was a pregnancy test carried out?
    Item
    Was a pregnancy test carried out?
    boolean
    C0032976 (UMLS CUI [1])
    If no pregnancy test was carried out, specify reason
    Item
    If no pregnancy test was carried out, specify reason
    text
    C0032976 (UMLS CUI [1,1])
    C2826287 (UMLS CUI [1,2])
    Date of pregnancy test
    Item
    Date of pregnancy test
    date
    C0032976 (UMLS CUI [1,1])
    C0011008 (UMLS CUI [1,2])
    Item
    Result of Pregnancy Test
    integer
    C0427777 (UMLS CUI [1])
    Result of Pregnancy Test
    Code List
    Result of Pregnancy Test
    CL Item
    Positive (1)
    CL Item
    Negative (2)
    Volver a la parte superior de la página 

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