0 Bedömningar
ID

37740

Beskrivning

Study ID: 104864/517 Clinical Study ID: 104864/517 Study Title: A Phase I Study of Oral Topotecan as a Radiosensitizing Agent in Patients With Rectal Cancer Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00158886 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: Topotecan + Radiation therapy Trade Name: N/A Study Indication: Rectal Cancer, Carcinoma, Renal Cell

Nyckelord

Versioner (1)
  1. 21.08.19 21.08.19 -
Rättsinnehavare

GlaxoSmithKline

Uppladdad den

21. August 2019

DOI

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Licens

Creative Commons BY-NC 3.0
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    Oral Topotecan as Radiosensitizing Agent in Patients with Rectal Cancer; NCT00158886

    Engelsk

    Patient Log

    1 Formulär  
    1. StudyEvent: ODM
      1. Patient Log
    Administrative Data
    Beskrivning

    Administrative Data

    Alias
    UMLS CUI-1
    C1320722
    Center number
    Beskrivning

    Study Coordinating Center, Identification number

    Datatyp

    integer

    Alias
    UMLS CUI [1,1]
    C2825181
    UMLS CUI [1,2]
    C1300638
    Patient Log
    Beskrivning

    Patient Log

    Alias
    UMLS CUI-1
    C0030705
    UMLS CUI-2
    C2828389
    Investigator
    Beskrivning

    Patients, Exclusion, Investigator Name

    Datatyp

    text

    Alias
    UMLS CUI [1,1]
    C0030705
    UMLS CUI [1,2]
    C2828389
    UMLS CUI [1,3]
    C2826892
    Patient Initials
    Beskrivning

    Patients, Exclusion, Person Initials

    Datatyp

    text

    Alias
    UMLS CUI [1,1]
    C0030705
    UMLS CUI [1,2]
    C2828389
    UMLS CUI [1,3]
    C2986440
    Interview Date
    Beskrivning

    Patients, Exclusion, patient interview, Date in time

    Datatyp

    date

    Alias
    UMLS CUI [1,1]
    C0030705
    UMLS CUI [1,2]
    C2828389
    UMLS CUI [1,3]
    C0683518
    UMLS CUI [1,4]
    C0011008
    Reason for Exclusion
    Beskrivning

    Patients, Exclusion, Reason and justification

    Datatyp

    text

    Alias
    UMLS CUI [1,1]
    C0030705
    UMLS CUI [1,2]
    C2828389
    UMLS CUI [1,3]
    C0566251
    Tillbaka till toppen

    Similar models

    Patient Log

    1 Formulär
    1. StudyEvent: ODM
      1. Patient Log
    Name
    Typ
    Description | Question | Decode (Coded Value)
    Datatyp
    Alias
    Item Group
    Administrative Data
    C1320722 (UMLS CUI-1)
    Study Coordinating Center, Identification number
    Item
    Center number
    integer
    C2825181 (UMLS CUI [1,1])
    C1300638 (UMLS CUI [1,2])
    Item Group
    Patient Log
    C0030705 (UMLS CUI-1)
    C2828389 (UMLS CUI-2)
    Patients, Exclusion, Investigator Name
    Item
    Investigator
    text
    C0030705 (UMLS CUI [1,1])
    C2828389 (UMLS CUI [1,2])
    C2826892 (UMLS CUI [1,3])
    Patients, Exclusion, Person Initials
    Item
    Patient Initials
    text
    C0030705 (UMLS CUI [1,1])
    C2828389 (UMLS CUI [1,2])
    C2986440 (UMLS CUI [1,3])
    Patients, Exclusion, patient interview, Date in time
    Item
    Interview Date
    date
    C0030705 (UMLS CUI [1,1])
    C2828389 (UMLS CUI [1,2])
    C0683518 (UMLS CUI [1,3])
    C0011008 (UMLS CUI [1,4])
    Patients, Exclusion, Reason and justification
    Item
    Reason for Exclusion
    text
    C0030705 (UMLS CUI [1,1])
    C2828389 (UMLS CUI [1,2])
    C0566251 (UMLS CUI [1,3])
    Tillbaka till toppen 

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