0 Evaluaciones
ID

24369

Descripción

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.

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Versiones (1)
  1. 30/7/17 30/7/17 -
Titular de derechos de autor

GlaxoSmithKline

Subido en

30 de julio de 2017

DOI

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Licencia

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

    Inglés

    Study Conclusion End of Study

    1 formularios  
    STUDY CONCLUSION
    Descripción

    STUDY CONCLUSION

    Alias
    UMLS CUI-1
    C1707478 (Conclusion)
    UMLS CUI-2
    C0008972 (Clinical Research)
    Subject ID
    Descripción

    Subject ID

    Tipo de datos

    text

    Alias
    UMLS CUI [1]
    C2348585 (Clinical Trial Subject Unique Identifier)
    Date of subject completion or withdrawal
    Descripción

    Date of subject completion or withdrawal

    Tipo de datos

    date

    Alias
    UMLS CUI [1]
    C2983670 (Study End Date)
    Was the subject withdrawn from the study?
    Descripción

    Study Subject Participation Status

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C2348568 (Study Subject Participation Status)
    The primary reason for withdrawal:
    Descripción

    reason study conclusion

    Tipo de datos

    text

    Alias
    UMLS CUI [1,1]
    C0392360 (Indication of (contextual qualifier))
    SNOMED
    230165009
    LOINC
    MTHU008319
    UMLS CUI [1,2]
    C1707478 (Conclusion)
    UMLS CUI [1,3]
    C0008972 (Clinical Research)
    If other, please specify
    Descripción

    Other

    Tipo de datos

    text

    Alias
    UMLS CUI [1]
    C0205394 (Other)
    SNOMED
    74964007
    LOINC
    LP21049-9
    PREGNANCY INFORMATION
    Descripción

    PREGNANCY INFORMATION

    Alias
    UMLS CUI-1
    C0032961 (Pregnancy)
    SNOMED
    289908002
    LOINC
    LP75920-6
    UMLS CUI-2
    C1533716 (Information)
    Did the subject become pregnant during the study?
    Descripción

    pregnancy

    Tipo de datos

    text

    Alias
    UMLS CUI [1]
    C0032961 (Pregnancy)
    SNOMED
    289908002
    LOINC
    LP75920-6
    Volver a la parte superior de la página

    Similar models

    Study Conclusion End of Study

    1 formularios
    Name
    Tipo
    Description | Question | Decode (Coded Value)
    Tipo de datos
    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))
    Volver a la parte superior de la página 

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