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ID

22593

Beschrijving

Terms of use: You may not use this document or the information contained herein to a regulatory authority in connection with an application for a marketing authorization or any other regulatory submission without the express written consent of Roche Study #: FVF4168g Drug: Ranibizumab Study Title: A Phase III, Double-Masked, Multicenter, Randomized, Sham-Controlled Study Of The Efficacy And Safety Of Ranibizumab Injection In Subjects With Clinically Significant Macular Edema With Center Involvement Secondary To Diabetes Mellitus

Trefwoorden

  1. 08/06/17 08/06/17 -
Houder van rechten

Genentech, Inc.

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8 giugno 2017

DOI

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Licentie

Creative Commons BY-NC 3.0

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    SUBJECT ELIGIBILITY (SCREENING) CRFs Roche FVF4168G Macular Edema NCT00473330

    SUBJECT ELIGIBILITY (SCREENING) CRFs Roche FVF4168G Macular Edema NCT00473330

    Patient administration
    Beschrijving

    Patient administration

    Subject Number
    Beschrijving

    PT

    Datatype

    integer

    Alias
    UMLS CUI [1]
    C2348585 (Clinical Trial Subject Unique Identifier)
    Subject Initials:
    Beschrijving

    PTINIT

    Datatype

    text

    Alias
    UMLS CUI [1,1]
    C1997894 (Clinical trial participant (person))
    SNOMED
    428024001
    UMLS CUI [1,2]
    C2986440 (Person Initials)
    Report Date:
    Beschrijving

    VDT

    Datatype

    date

    Alias
    UMLS CUI [1,1]
    C1302584 (Date of report)
    SNOMED
    399651003
    SUBJECT ELIGIBILITY
    Beschrijving

    SUBJECT ELIGIBILITY

    Date Subject Signed Protocol Informed Consent:
    Beschrijving

    INFORM_CONSENT_DT

    Datatype

    date

    Alias
    UMLS CUI [1]
    C2985782 (Informed Consent Date)
    Did subject meet all eligibility criteria?
    Beschrijving

    If No: • Indicate the line number(s) (from worksheet) of eligibility criteria that was not met • Provide details of the deviation from the specified eligibility criteria • Indicate if waiver was given and the date granted

    Datatype

    integer

    Alias
    UMLS CUI [1]
    C1302261 (Patient eligible for clinical trial)
    SNOMED
    399223003
    Eligibility Criteria Not Met
    Beschrijving

    Eligibility Criteria Not Met

    Line Number(s) of Eligibility Criteria Not Met (e.g., E-3)
    Beschrijving

    CRIT_NOTMET

    Datatype

    text

    Alias
    UMLS CUI [1,1]
    C1516637 (Clinical Trial Eligibility Criteria)
    Details
    Beschrijving

    DEVIATION_DETAILS

    Datatype

    text

    Alias
    UMLS CUI [1,1]
    C1555471 (Not Eligible)
    UMLS CUI [1,2]
    C0566251 (Reason and justification)
    SNOMED
    288830005
    Was A Waiver Granted?
    Beschrijving

    APPROVAL

    Datatype

    boolean

    Alias
    UMLS CUI [1,1]
    C1707901 (Eligibility Waiver)
    If Yes, Date:
    Beschrijving

    APPROVAL_DT

    Datatype

    date

    Alias
    UMLS CUI [1,1]
    C1707901 (Eligibility Waiver)
    UMLS CUI [1,2]
    C0011008 (Date in time)
    SNOMED
    410671006

    Similar models

    SUBJECT ELIGIBILITY (SCREENING) CRFs Roche FVF4168G Macular Edema NCT00473330

    Name
    Type
    Description | Question | Decode (Coded Value)
    Datatype
    Alias
    Item Group
    Patient administration
    PT
    Item
    Subject Number
    integer
    C2348585 (UMLS CUI [1])
    PTINIT
    Item
    Subject Initials:
    text
    C1997894 (UMLS CUI [1,1])
    C2986440 (UMLS CUI [1,2])
    VDT
    Item
    Report Date:
    date
    C1302584 (UMLS CUI [1,1])
    Item Group
    SUBJECT ELIGIBILITY
    INFORM_CONSENT_DT
    Item
    Date Subject Signed Protocol Informed Consent:
    date
    C2985782 (UMLS CUI [1])
    Item
    Did subject meet all eligibility criteria?
    integer
    C1302261 (UMLS CUI [1])
    Code List
    Did subject meet all eligibility criteria?
    CL Item
    With Direction (1)
    CL Item
    Without Direction (2)
    Item Group
    Eligibility Criteria Not Met
    CRIT_NOTMET
    Item
    Line Number(s) of Eligibility Criteria Not Met (e.g., E-3)
    text
    C1516637 (UMLS CUI [1,1])
    DEVIATION_DETAILS
    Item
    Details
    text
    C1555471 (UMLS CUI [1,1])
    C0566251 (UMLS CUI [1,2])
    APPROVAL
    Item
    Was A Waiver Granted?
    boolean
    C1707901 (UMLS CUI [1,1])
    APPROVAL_DT
    Item
    If Yes, Date:
    date
    C1707901 (UMLS CUI [1,1])
    C0011008 (UMLS CUI [1,2])

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