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ID

27273

Beskrivning

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: Study Conclusion

Nyckelord

Versioner (1)
  1. 2017-11-06 2017-11-06 -
Rättsinnehavare

GlaxoSmithKline

Uppladdad den

6 november 2017

DOI

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Licens

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

    Engelsk

    Study Conclusion

    1 Formulär  
    1. StudyEvent: ODM
      1. Study Conclusion
    Study Conclusion
    Beskrivning

    Study Conclusion

    Alias
    UMLS CUI-1
    C2348568
    UMLS CUI-2
    C1707478
    UMLS CUI-3
    C0008976
    UMLS CUI-4
    C0035258
    Did the patient complete the study according to the protocol?
    Beskrivning

    End of Study

    Datatyp

    boolean

    Alias
    UMLS CUI [1,1]
    C2348568
    UMLS CUI [1,2]
    C0444496
    If ’No’, please mark the primary cause of withdrawal. (Mark one box only)
    Beskrivning

    primary cause of withdrawal

    Datatyp

    integer

    Alias
    UMLS CUI [1,1]
    C0422727
    UMLS CUI [1,2]
    C0392360
    Primary cause of withdrawal: If 'Other', please specify
    Beskrivning

    primary cause of withdrawal

    Datatyp

    text

    Alias
    UMLS CUI [1,1]
    C0422727
    UMLS CUI [1,2]
    C0392360
    Investigator’s Signature
    Beskrivning

    Investigator’s Signature

    Datatyp

    text

    Alias
    UMLS CUI [1]
    C2346576
    Investigator’s Signature Date
    Beskrivning

    Investigator’s Signature Date

    Datatyp

    date

    Alias
    UMLS CUI [1,1]
    C2346576
    UMLS CUI [1,2]
    C0011008
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    Similar models

    Study Conclusion

    1 Formulär
    1. StudyEvent: ODM
      1. Study Conclusion
    Name
    Typ
    Description | Question | Decode (Coded Value)
    Datatyp
    Alias
    Item Group
    Study Conclusion
    C2348568 (UMLS CUI-1)
    C1707478 (UMLS CUI-2)
    C0008976 (UMLS CUI-3)
    C0035258 (UMLS CUI-4)
    End of Study
    Item
    Did the patient complete the study according to the protocol?
    boolean
    C2348568 (UMLS CUI [1,1])
    C0444496 (UMLS CUI [1,2])
    Item
    If ’No’, please mark the primary cause of withdrawal. (Mark one box only)
    integer
    C0422727 (UMLS CUI [1,1])
    C0392360 (UMLS CUI [1,2])
    primary cause of withdrawal
    Code List
    If ’No’, please mark the primary cause of withdrawal. (Mark one box only)
    CL Item
    Adverse experience (please complete AE page)  (1)
    CL Item
    Insufficient therapeutic effect (2)
    CL Item
    Protocol deviation (including non-compliance) (3)
    CL Item
    Lost to follow-up (4)
    CL Item
    Other (5)
    primary cause of withdrawal
    Item
    Primary cause of withdrawal: If 'Other', please specify
    text
    C0422727 (UMLS CUI [1,1])
    C0392360 (UMLS CUI [1,2])
    Investigator’s Signature
    Item
    Investigator’s Signature
    text
    C2346576 (UMLS CUI [1])
    Investigator’s Signature Date
    Item
    Investigator’s Signature Date
    date
    C2346576 (UMLS CUI [1,1])
    C0011008 (UMLS CUI [1,2])
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