0 Beoordelingen
ID

29797

Beschrijving

Study ID: 101464 Clinical Study ID: SCA101464 Study Title: A Multicenter, Randomized, Double-Blind, Parallel Group Study to Evaluate the Efficacy and Safety of a Flexible Dose of Lamotrigine Compared to Placebo as an Adjunctive Therapy to an Atypical Antipsychotic Agent(s) in Subjects with Schizophrenia Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00086593 https://clinicaltrials.gov/ct2/show/NCT00086593 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 3 Study Recruitment Status: Completed Generic Name: lamotrigine Study Indication: Lamictal XR,Lamictal,LAMICTIN This ODM form contains End of Study Record / Hospitalization and Status of Treatment Blind.

Link

https://clinicaltrials.gov/ct2/show/NCT00086593

Trefwoorden

Versies (1)
  1. 19-04-18 19-04-18 - Sarah Riepenhausen
Houder van rechten

GlaxoSmithKline

Geüploaded op

19 april 2018

DOI

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Licentie

Creative Commons BY-NC 3.0
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    Evaluation of a Flexible Dose of Lamotrigine Compared to Placebo as an Adjunctive to Atypical Antipsychotic Agents in Schizophrenia NCT00086593

    Engels

    End of Study Record / Hospitalization and Status of Treatment Blind

    1 Formulieren  
    End of Study Record
    Beschrijving

    End of Study Record

    Alias
    UMLS CUI-1
    C0008972
    UMLS CUI-2
    C0444930
    Date of subject completion or discontinuation from the study
    Beschrijving

    Record the date of the last follow-up visit or contact. Completion of the study is defined as a subject who completes the Week 12 End of Study Visit.

    Datatype

    date

    Alias
    UMLS CUI [1,1]
    C2348577
    UMLS CUI [1,2]
    C0011008
    UMLS CUI [2,1]
    C0457454
    UMLS CUI [2,2]
    C0011008
    Did the subject become pregnant during the study?
    Beschrijving

    This question must be answered for all subjects. For females not of childbearing potential or males, mark NOT APPLICABLE. If no pregnancy was known before a subject was lost to follow-up, mark NO. If the subject became pregnant before either premature discontinuation from the study or completion of the study, mark YES and record details on PREGNANCY NOTIFICATION FORM.

    Datatype

    text

    Alias
    UMLS CUI [1,1]
    C0032961
    UMLS CUI [1,2]
    C0008976
    Did the subject discontinue the study prematurely?
    Beschrijving

    Premature Study Discontinuation

    Datatype

    text

    Alias
    UMLS CUI [1,1]
    C0457454
    UMLS CUI [1,2]
    C2348568
    If yes, mark the primary reason for discontinuation
    Beschrijving

    If A: Record details on NON-SERIOUS ADVERSE EVENTS or SERIOUS ADVERSE EVENT page as appropriate.

    Datatype

    text

    Alias
    UMLS CUI [1,1]
    C0392360
    UMLS CUI [1,2]
    C0457454
    UMLS CUI [1,3]
    C0008976
    If other reason for discontinuation, specify:
    Beschrijving

    Reason for discontinuation

    Datatype

    text

    Alias
    UMLS CUI [1,1]
    C0392360
    UMLS CUI [1,2]
    C0457454
    UMLS CUI [1,3]
    C0008976
    Hospitalization Status
    Beschrijving

    Hospitalization Status

    Alias
    UMLS CUI-1
    C0019993
    UMLS CUI-2
    C0449438
    Did the subject admit or discharge from the hospital?
    Beschrijving

    Hospitalization

    Datatype

    text

    Alias
    UMLS CUI [1]
    C0019993
    Date of Admittance 1
    Beschrijving

    Date of Admittance

    Datatype

    date

    Alias
    UMLS CUI [1]
    C0806429
    Date of discharge 1
    Beschrijving

    Date of discharge

    Datatype

    date

    Alias
    UMLS CUI [1]
    C2361123
    Date of Admittance 2
    Beschrijving

    Date of Admittance

    Datatype

    date

    Alias
    UMLS CUI [1]
    C0806429
    Date of discharge 2
    Beschrijving

    Date of discharge

    Datatype

    date

    Alias
    UMLS CUI [1]
    C2361123
    Status of Treatment Blind
    Beschrijving

    Status of Treatment Blind

    Alias
    UMLS CUI-1
    C2347038
    UMLS CUI-2
    C0449438
    Was the treatment blind for this subject broken during the study?
    Beschrijving

    If YES, check that a date and reason are present and that the appropriate NON-SERIOUS ADVERSE EVENT, SERIOUS ADVERSE EVENT, END OF STUDY RECORD, and /or INVESTIGATIONAL PRODUCT pages are completed.

    Datatype

    text

    Alias
    UMLS CUI [1]
    C3897431
    If treatment blind was broken, give the date:
    Beschrijving

    Date of Treatment Blind breaking

    Datatype

    date

    Alias
    UMLS CUI [1,1]
    C3897431
    UMLS CUI [1,2]
    C0011008
    If treatment blind was broken, give a reason:
    Beschrijving

    Reason for Treatment Blind breaking

    Datatype

    text

    Alias
    UMLS CUI [1,1]
    C3897431
    UMLS CUI [1,2]
    C0392360
    If there was another reason for treatment blind breaking, specify:
    Beschrijving

    Other Reason

    Datatype

    text

    Alias
    UMLS CUI [1,1]
    C3840932
    UMLS CUI [1,2]
    C3897431
    Investigator's Statement
    Beschrijving

    Investigator's Statement

    Alias
    UMLS CUI-1
    C0008961
    UMLS CUI-2
    C1710187
    I confirm that I have carefully examined all entries on the Case Report Form for this subject. All information entered by myself or my colleagues is, to the best of my knowledge, correct as of the date below.
    Beschrijving

    Investigator's signature

    Datatype

    text

    Alias
    UMLS CUI [1]
    C2346576
    Date of signature
    Beschrijving

    Date of signature

    Datatype

    date

    Alias
    UMLS CUI [1,1]
    C2346576
    UMLS CUI [1,2]
    C0011008
    Investigator's Name (Print)
    Beschrijving

    Investigator's Name

    Datatype

    text

    Alias
    UMLS CUI [1]
    C2826892
    Terug naar het begin van de pagina

    Similar models

    End of Study Record / Hospitalization and Status of Treatment Blind

    1 Formulieren
    Name
    Type
    Description | Question | Decode (Coded Value)
    Datatype
    Alias
    Item Group
    End of Study Record
    C0008972 (UMLS CUI-1)
    C0444930 (UMLS CUI-2)
    Date of subject completion or discontinuation from the study
    Item
    Date of subject completion or discontinuation from the study
    date
    C2348577 (UMLS CUI [1,1])
    C0011008 (UMLS CUI [1,2])
    C0457454 (UMLS CUI [2,1])
    C0011008 (UMLS CUI [2,2])
    Item
    Did the subject become pregnant during the study?
    text
    C0032961 (UMLS CUI [1,1])
    C0008976 (UMLS CUI [1,2])
    Pregnancy during study
    Code List
    Did the subject become pregnant during the study?
    CL Item
    Not applicable (X)
    CL Item
    No (N)
    CL Item
    Yes (Y)
    Item
    Did the subject discontinue the study prematurely?
    text
    C0457454 (UMLS CUI [1,1])
    C2348568 (UMLS CUI [1,2])
    Premature Study Discontinuation
    Code List
    Did the subject discontinue the study prematurely?
    CL Item
    Yes (Y)
    CL Item
    No (N)
    Item
    If yes, mark the primary reason for discontinuation
    text
    C0392360 (UMLS CUI [1,1])
    C0457454 (UMLS CUI [1,2])
    C0008976 (UMLS CUI [1,3])
    Reason for discontinuation
    Code List
    If yes, mark the primary reason for discontinuation
    CL Item
    Adverse Event (A)
    CL Item
    Consent withdrawn (C)
    CL Item
    Lost to Follow up (L)
    CL Item
    Protocol violation (P)
    CL Item
    Lack of Efficacy (E)
    CL Item
    Other (X)
    Reason for discontinuation
    Item
    If other reason for discontinuation, specify:
    text
    C0392360 (UMLS CUI [1,1])
    C0457454 (UMLS CUI [1,2])
    C0008976 (UMLS CUI [1,3])
    Item Group
    Hospitalization Status
    C0019993 (UMLS CUI-1)
    C0449438 (UMLS CUI-2)
    Item
    Did the subject admit or discharge from the hospital?
    text
    C0019993 (UMLS CUI [1])
    Hospitalization
    Code List
    Did the subject admit or discharge from the hospital?
    CL Item
    Yes (Y)
    CL Item
    No (N)
    Date of Admittance
    Item
    Date of Admittance 1
    date
    C0806429 (UMLS CUI [1])
    Date of discharge
    Item
    Date of discharge 1
    date
    C2361123 (UMLS CUI [1])
    Date of Admittance
    Item
    Date of Admittance 2
    date
    C0806429 (UMLS CUI [1])
    Date of discharge
    Item
    Date of discharge 2
    date
    C2361123 (UMLS CUI [1])
    Item Group
    Status of Treatment Blind
    C2347038 (UMLS CUI-1)
    C0449438 (UMLS CUI-2)
    Item
    Was the treatment blind for this subject broken during the study?
    text
    C3897431 (UMLS CUI [1])
    Treatment Blind broken
    Code List
    Was the treatment blind for this subject broken during the study?
    CL Item
    Yes (Y)
    CL Item
    No (N)
    Date of Treatment Blind breaking
    Item
    If treatment blind was broken, give the date:
    date
    C3897431 (UMLS CUI [1,1])
    C0011008 (UMLS CUI [1,2])
    Item
    If treatment blind was broken, give a reason:
    text
    C3897431 (UMLS CUI [1,1])
    C0392360 (UMLS CUI [1,2])
    Reason for Treatment Blind breaking
    Code List
    If treatment blind was broken, give a reason:
    CL Item
    Medical emergency requiring identity of investigational product for further treatment (E)
    CL Item
    Other (X)
    Other Reason
    Item
    If there was another reason for treatment blind breaking, specify:
    text
    C3840932 (UMLS CUI [1,1])
    C3897431 (UMLS CUI [1,2])
    Item Group
    Investigator's Statement
    C0008961 (UMLS CUI-1)
    C1710187 (UMLS CUI-2)
    Investigator's signature
    Item
    I confirm that I have carefully examined all entries on the Case Report Form for this subject. All information entered by myself or my colleagues is, to the best of my knowledge, correct as of the date below.
    text
    C2346576 (UMLS CUI [1])
    Date of signature
    Item
    Date of signature
    date
    C2346576 (UMLS CUI [1,1])
    C0011008 (UMLS CUI [1,2])
    Investigator's Name
    Item
    Investigator's Name (Print)
    text
    C2826892 (UMLS CUI [1])
    Terug naar het begin van de pagina 

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