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ID

27191

Description

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: Medical Procedures

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Versions (1)
  1. 3/11/17 3/11/17 -
Détendeur de droits

GlaxoSmithKline

Téléchargé le

3 de noviembre de 2017

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0
Modèle Commentaires :

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    GSK Ropinirole in Patients Suffering from Restless Legs Syndrome 101468/188

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    Medical Procedures

    1 Formulaires  
    1. StudyEvent: ODM
      1. Medical Procedures
    Medical Procedures
    Description

    Medical Procedures

    Alias
    UMLS CUI-1
    C0199171
    UMLS CUI-2
    C0087111
    UMLS CUI-3
    C0430022
    UMLS CUI-4
    C0543467
    Have any non-medication, therapeutic, diagnostic or surgical procedures been performed since the last clinic visit (non-PSG)? All indications for procedures should be recorded in the Adverse Experience and/or SAE section as appropriate.
    Description

    If "Yes", please record details below using standard medical terminology.

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0199171
    UMLS CUI [2]
    C0087111
    UMLS CUI [3]
    C0430022
    UMLS CUI [4]
    C0543467
    Procedure
    Description

    Procedure

    Type de données

    text

    Alias
    UMLS CUI [1,1]
    C0199171
    UMLS CUI [1,2]
    C0332307
    Indication for procedure
    Description

    Indication for procedure

    Type de données

    text

    Alias
    UMLS CUI [1,1]
    C0199171
    UMLS CUI [1,2]
    C3146298
    Procedure Start Date
    Description

    Procedure Start Date

    Type de données

    date

    Alias
    UMLS CUI [1,1]
    C0199171
    UMLS CUI [1,2]
    C0808070
    Procedure End Date
    Description

    Procedure End Date

    Type de données

    date

    Alias
    UMLS CUI [1,1]
    C0199171
    UMLS CUI [1,2]
    C0806020
    Retour au début de la page

    Similar models

    Medical Procedures

    1 Formulaires
    1. StudyEvent: ODM
      1. Medical Procedures
    Name
    Type
    Description | Question | Decode (Coded Value)
    Type de données
    Alias
    Item Group
    Medical Procedures
    C0199171 (UMLS CUI-1)
    C0087111 (UMLS CUI-2)
    C0430022 (UMLS CUI-3)
    C0543467 (UMLS CUI-4)
    Medical Procedures
    Item
    Have any non-medication, therapeutic, diagnostic or surgical procedures been performed since the last clinic visit (non-PSG)? All indications for procedures should be recorded in the Adverse Experience and/or SAE section as appropriate.
    boolean
    C0199171 (UMLS CUI [1])
    C0087111 (UMLS CUI [2])
    C0430022 (UMLS CUI [3])
    C0543467 (UMLS CUI [4])
    Procedure
    Item
    Procedure
    text
    C0199171 (UMLS CUI [1,1])
    C0332307 (UMLS CUI [1,2])
    Indication for procedure
    Item
    Indication for procedure
    text
    C0199171 (UMLS CUI [1,1])
    C3146298 (UMLS CUI [1,2])
    Procedure Start Date
    Item
    Procedure Start Date
    date
    C0199171 (UMLS CUI [1,1])
    C0808070 (UMLS CUI [1,2])
    Procedure End Date
    Item
    Procedure End Date
    date
    C0199171 (UMLS CUI [1,1])
    C0806020 (UMLS CUI [1,2])
    Retour au début de la page 

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