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ID

27684

Description

Study ID: 103094 Clinical Study ID: ARI103094 Study Title: ARI103094-Follow-Up Study for REDUCE Study Subjects Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00883909 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 3 Study Recruitment Status: Completed Generic Name: dutasteride Trade Name: Zytefor,Zyfetor,Duagen,Avolve,Avodart,Avidart Study Indication: Neoplasms, Prostate CRF Seiten: 934-977

Mots-clés

  1. 15/11/2017 15/11/2017 -
  2. 26/11/2017 26/11/2017 -
Détendeur de droits

GlaxoSmithKline

Téléchargé le

26 novembre 2017

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0

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    Investigator data Log GSK study Prostatic neoplasms NCT00883909

    Investigator data Log GSK study Prostatic neoplasms NCT00883909

    Administrative data
    Description

    Administrative data

    Alias
    UMLS CUI-1
    C1320722
    Session number
    Description

    Session number

    Type de données

    integer

    Alias
    UMLS CUI [1,1]
    C1883017
    UMLS CUI [1,2]
    C0750480
    Subject number
    Description

    Subject number

    Type de données

    text

    Alias
    UMLS CUI [1]
    C2348585
    Investigator Comment Log
    Description

    Investigator Comment Log

    Alias
    UMLS CUI-1
    C0008961
    UMLS CUI-2
    C0947611
    Date of comment
    Description

    Date of comment

    Type de données

    date

    Alias
    UMLS CUI [1,1]
    C0011008
    UMLS CUI [1,2]
    C0947611
    CRF page number if applicable
    Description

    page number CRF

    Type de données

    integer

    Alias
    UMLS CUI [1,1]
    C1704732
    UMLS CUI [1,2]
    C1516308
    Comment
    Description

    Comment

    Type de données

    text

    Alias
    UMLS CUI [1]
    C0947611
    Investigator’s Statement
    Description

    Investigator’s Statement

    Alias
    UMLS CUI-1
    C0008961
    UMLS CUI-2
    C1710187
    Date
    Description

    Check that the date of signature is on or after the completion of Visit 10.

    Type de données

    date

    Alias
    UMLS CUI [1]
    C0011008
    Investigator’s Signature
    Description

    Sign and date this page after all relevant CRF pages, including outstanding test results, are completed.

    Type de données

    text

    Alias
    UMLS CUI [1]
    C2346576
    Investigator’s Name - Print
    Description

    Investigator Name

    Type de données

    text

    Alias
    UMLS CUI [1]
    C2826892

    Similar models

    Investigator data Log GSK study Prostatic neoplasms NCT00883909

    Name
    Type
    Description | Question | Decode (Coded Value)
    Type de données
    Alias
    Item Group
    Administrative data
    C1320722 (UMLS CUI-1)
    Session number
    Item
    Session number
    integer
    C1883017 (UMLS CUI [1,1])
    C0750480 (UMLS CUI [1,2])
    Subject number
    Item
    Subject number
    text
    C2348585 (UMLS CUI [1])
    Item Group
    Investigator Comment Log
    C0008961 (UMLS CUI-1)
    C0947611 (UMLS CUI-2)
    Date of comment
    Item
    Date of comment
    date
    C0011008 (UMLS CUI [1,1])
    C0947611 (UMLS CUI [1,2])
    page number CRF
    Item
    CRF page number if applicable
    integer
    C1704732 (UMLS CUI [1,1])
    C1516308 (UMLS CUI [1,2])
    Comment
    Item
    Comment
    text
    C0947611 (UMLS CUI [1])
    Item Group
    Investigator’s Statement
    C0008961 (UMLS CUI-1)
    C1710187 (UMLS CUI-2)
    Date
    Item
    Date
    date
    C0011008 (UMLS CUI [1])
    Investigator Signature
    Item
    Investigator’s Signature
    text
    C2346576 (UMLS CUI [1])
    Investigator Name
    Item
    Investigator’s Name - Print
    text
    C2826892 (UMLS CUI [1])

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