0 Bedömningar
ID

24369

Beskrivning

Study part: Study Conclusion End of Study.An Open-Label Extension phase 3 Study with REQUIP (ropinirole) CR for Subjects from Studies 101468/165, 101468/168 and 101468/169 Patient Level Data. Study ID:101468/248, Clinical Study ID: 101468/248.

Nyckelord

Versioner (1)
  1. 2017-07-30 2017-07-30 -
Rättsinnehavare

GlaxoSmithKline

Uppladdad den

30 juli 2017

DOI

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Licens

Creative Commons BY-NC 3.0
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    Study Conclusion End of Study Ropinirole NCT00632736

    Engelsk

    Study Conclusion End of Study

    1 Formulär  
    STUDY CONCLUSION
    Beskrivning

    STUDY CONCLUSION

    Alias
    UMLS CUI-1
    C1707478
    UMLS CUI-2
    C0008972
    Subject ID
    Beskrivning

    Subject ID

    Datatyp

    text

    Alias
    UMLS CUI [1]
    C2348585
    Date of subject completion or withdrawal
    Beskrivning

    Date of subject completion or withdrawal

    Datatyp

    date

    Alias
    UMLS CUI [1]
    C2983670
    Was the subject withdrawn from the study?
    Beskrivning

    Study Subject Participation Status

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C2348568
    The primary reason for withdrawal:
    Beskrivning

    reason study conclusion

    Datatyp

    text

    Alias
    UMLS CUI [1,1]
    C0392360
    UMLS CUI [1,2]
    C1707478
    UMLS CUI [1,3]
    C0008972
    If other, please specify
    Beskrivning

    Other

    Datatyp

    text

    Alias
    UMLS CUI [1]
    C0205394
    PREGNANCY INFORMATION
    Beskrivning

    PREGNANCY INFORMATION

    Alias
    UMLS CUI-1
    C0032961
    UMLS CUI-2
    C1533716
    Did the subject become pregnant during the study?
    Beskrivning

    pregnancy

    Datatyp

    text

    Alias
    UMLS CUI [1]
    C0032961
    Tillbaka till toppen

    Similar models

    Study Conclusion End of Study

    1 Formulär
    Name
    Typ
    Description | Question | Decode (Coded Value)
    Datatyp
    Alias
    Item Group
    STUDY CONCLUSION
    C1707478 (UMLS CUI-1)
    C0008972 (UMLS CUI-2)
    Subject ID
    Item
    Subject ID
    text
    C2348585 (UMLS CUI [1])
    Date of subject completion or withdrawal
    Item
    Date of subject completion or withdrawal
    date
    C2983670 (UMLS CUI [1])
    Study Subject Participation Status
    Item
    Was the subject withdrawn from the study?
    boolean
    C2348568 (UMLS CUI [1])
    Item
    The primary reason for withdrawal:
    text
    C0392360 (UMLS CUI [1,1])
    C1707478 (UMLS CUI [1,2])
    C0008972 (UMLS CUI [1,3])
    reason study conclusion
    Code List
    The primary reason for withdrawal:
    CL Item
    Adverse event (record details on the Non-Serious Adverse Event or Serious Adverse Event pages as appropriate) (Adverse event (record details on the Non-Serious Adverse Event or Serious Adverse Event pages as appropriate))
    C0877248 (UMLS CUI-1)
    CL Item
    Lost to follow-up (Lost to follow-up)
    C1302313 (UMLS CUI-1)
    CL Item
    Protocol violation (Protocol violation)
    C1709750 (UMLS CUI-1)
    CL Item
    Subject decided to withdraw from the study (Subject decided to withdraw from the study)
    C2348571 (UMLS CUI-1)
    CL Item
    Lack of efficacy (Lack of efficacy)
    C0235828 (UMLS CUI-1)
    CL Item
    Sponsor terminated study (Sponsor terminated study)
    C1710224 (UMLS CUI-1)
    CL Item
    Disease progression (Disease progression)
    C0242656 (UMLS CUI-1)
    CL Item
    Other, specify (Other, specify)
    C0205394 (UMLS CUI-1)
    Other
    Item
    If other, please specify
    text
    C0205394 (UMLS CUI [1])
    Item Group
    PREGNANCY INFORMATION
    C0032961 (UMLS CUI-1)
    C1533716 (UMLS CUI-2)
    Item
    Did the subject become pregnant during the study?
    text
    C0032961 (UMLS CUI [1])
    pregnancy
    Code List
    Did the subject become pregnant during the study?
    CL Item
    Yes (Yes)
    CL Item
    No (No)
    CL Item
    Not Applicable (not of childbearing potential or male) (Not Applicable (not of childbearing potential or male))
    Tillbaka till toppen 

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