0 Beoordelingen
ID

36217

Beschrijving

Study ID: 101963 Clinical Study ID: SCA101963 Study Title: A randomised, blinded, parallel group study to investigate the potential pharmacokinetic interaction between lamotrigine and risperidone in healthy, non-smoking, male volunteers. Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: lamotrigine Trade Name: Lamictal XR,Lamictal,LAMICTIN Study Indication: Schizophrenia

Trefwoorden

Versies (1)
  1. 22-04-19 22-04-19 -
Houder van rechten

GlaxoSmithKline

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22 april 2019

DOI

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Licentie

Creative Commons BY-NC 3.0
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    Potential Pharmacokinetic Interaction between Lamotrigine and Risperidone; 101963

    Engels

    Study Conclusion

    1 Formulieren  
    1. StudyEvent: ODM
      1. Study Conclusion
    Administrative Data
    Beschrijving

    Administrative Data

    Alias
    UMLS CUI-1
    C1320722
    Subject Identifier
    Beschrijving

    Clinical Trial Subject Unique Identifier

    Datatype

    integer

    Alias
    UMLS CUI [1]
    C2348585
    Study Conclusion
    Beschrijving

    Study Conclusion

    Alias
    UMLS CUI-1
    C1707478
    UMLS CUI-2
    C0008972
    Date of subject completion or withdrawal
    Beschrijving

    Report completion date; Patient withdrawn from trial, Date in time

    Datatype

    date

    Alias
    UMLS CUI [1]
    C1549507
    UMLS CUI [2,1]
    C0422727
    UMLS CUI [2,2]
    C0011008
    Time of withdrawal
    Beschrijving

    Withdraw, Time

    Datatype

    time

    Alias
    UMLS CUI [1,1]
    C2349954
    UMLS CUI [1,2]
    C0040223
    Was the subject withdrawn from the study?
    Beschrijving

    Subject withdrawn from trial

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0422727
    If Yes, tick he primary reason for withdrawal:
    Beschrijving

    Subject withdrawn from trial, Indication

    Datatype

    text

    Alias
    UMLS CUI [1,1]
    C0422727
    UMLS CUI [1,2]
    C3146298
    Terug naar het begin van de pagina

    Similar models

    Study Conclusion

    1 Formulieren
    1. StudyEvent: ODM
      1. Study Conclusion
    Name
    Type
    Description | Question | Decode (Coded Value)
    Datatype
    Alias
    Item Group
    Administrative Data
    C1320722 (UMLS CUI-1)
    Clinical Trial Subject Unique Identifier
    Item
    Subject Identifier
    integer
    C2348585 (UMLS CUI [1])
    Item Group
    Study Conclusion
    C1707478 (UMLS CUI-1)
    C0008972 (UMLS CUI-2)
    Report completion date; Patient withdrawn from trial, Date in time
    Item
    Date of subject completion or withdrawal
    date
    C1549507 (UMLS CUI [1])
    C0422727 (UMLS CUI [2,1])
    C0011008 (UMLS CUI [2,2])
    Withdraw, Time
    Item
    Time of withdrawal
    time
    C2349954 (UMLS CUI [1,1])
    C0040223 (UMLS CUI [1,2])
    Subject withdrawn from trial
    Item
    Was the subject withdrawn from the study?
    boolean
    C0422727 (UMLS CUI [1])
    Item
    If Yes, tick he primary reason for withdrawal:
    text
    C0422727 (UMLS CUI [1,1])
    C3146298 (UMLS CUI [1,2])
    Subject withdrawn from trial, Indication
    Code List
    If Yes, tick he primary reason for withdrawal:
    CL Item
    Adverse event  (1)
    CL Item
    Lost to follow-up (2)
    CL Item
    Protocol violation (3)
    CL Item
    Subject decided to withdraw from the study (4)
    CL Item
    Sponsor terminated study (5)
    CL Item
    Other (6)
    Terug naar het begin van de pagina 

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