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ID

31176

Description

Study ID: 104505 Clinical Study ID: BEX104505 Study Title: Phase II Study of Iodine 131 Anti B1 Antibody for 1st or 2nd Relapsed Indolent B-Cell Lymphomas or B-Cell Lymphomas That Have Transformed to a More Aggressive Histology Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00950755 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 2 Study Recruitment Status: Completed Generic Name: tositumomab Trade Name: Bexxar Study Indication: Lymphoma, Non-Hodgkin

Mots-clés

  1. 25/07/2018 25/07/2018 -
Détendeur de droits

see clinicaltrials.gov

Téléchargé le

25 juillet 2018

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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    Iodine 131 B1 Antibody for B-Cell Lymphomas NCT00950755

    Notification of Patient Death

    Administrative Data
    Description

    Administrative Data

    Alias
    UMLS CUI-1
    C1320722
    Site Number
    Description

    Site number

    Type de données

    text

    Alias
    UMLS CUI [1,1]
    C0018704
    UMLS CUI [1,2]
    C0600091
    Patient Number
    Description

    Patient Number

    Type de données

    text

    Alias
    UMLS CUI [1]
    C1830427
    Patient Initials
    Description

    Patient Initials

    Type de données

    text

    Alias
    UMLS CUI [1]
    C2986440
    Patient Death
    Description

    Patient Death

    Alias
    UMLS CUI-1
    C0011065
    Date of death
    Description

    Date of death

    Type de données

    date

    Alias
    UMLS CUI [1]
    C1148348
    Cause of death (check one)
    Description

    Cause of death

    Type de données

    text

    Alias
    UMLS CUI [1]
    C0007465
    If cause of death was related to complications of treatment, please describe or reference forms on which information was recorded.
    Description

    Complications of treatment

    Type de données

    text

    Alias
    UMLS CUI [1,1]
    C0087111
    UMLS CUI [1,2]
    C0009566
    Relations of study drug to patients death
    Description

    Study drug relation to death

    Type de données

    text

    Alias
    UMLS CUI [1,1]
    C0011065
    UMLS CUI [1,2]
    C0304229
    Source of information concerning death of patient (check all that apply)
    Description

    Patient death; Source of Information

    Type de données

    text

    Alias
    UMLS CUI [1,1]
    C0011065
    UMLS CUI [1,2]
    C1955348
    UMLS CUI [1,3]
    C0449416

    Similar models

    Notification of Patient Death

    Name
    Type
    Description | Question | Decode (Coded Value)
    Type de données
    Alias
    Item Group
    Administrative Data
    C1320722 (UMLS CUI-1)
    Site number
    Item
    Site Number
    text
    C0018704 (UMLS CUI [1,1])
    C0600091 (UMLS CUI [1,2])
    Patient Number
    Item
    Patient Number
    text
    C1830427 (UMLS CUI [1])
    Patient Initials
    Item
    Patient Initials
    text
    C2986440 (UMLS CUI [1])
    Item Group
    Patient Death
    C0011065 (UMLS CUI-1)
    Date of death
    Item
    Date of death
    date
    C1148348 (UMLS CUI [1])
    Item
    Cause of death (check one)
    text
    C0007465 (UMLS CUI [1])
    Code List
    Cause of death (check one)
    CL Item
    Progression of lymphoma (Progression of lymphoma)
    CL Item
    Complications related to drug (complete adverse Experiences form) (Complications related to drug (complete adverse Experiences form))
    CL Item
    Other (specify) (Other (specify))
    Complications of treatment
    Item
    If cause of death was related to complications of treatment, please describe or reference forms on which information was recorded.
    text
    C0087111 (UMLS CUI [1,1])
    C0009566 (UMLS CUI [1,2])
    Item
    Relations of study drug to patients death
    text
    C0011065 (UMLS CUI [1,1])
    C0304229 (UMLS CUI [1,2])
    Code List
    Relations of study drug to patients death
    CL Item
    None (None)
    CL Item
    Remote (Remote)
    CL Item
    Possible (Possible)
    CL Item
    Probable (Probable)
    Item
    Source of information concerning death of patient (check all that apply)
    text
    C0011065 (UMLS CUI [1,1])
    C1955348 (UMLS CUI [1,2])
    C0449416 (UMLS CUI [1,3])
    Code List
    Source of information concerning death of patient (check all that apply)
    CL Item
    Hospital physician (Hospital physician)
    CL Item
    Patient's physician (Patient's physician)
    CL Item
    Family (Family)
    CL Item
    Newspaper (obituary) (Newspaper (obituary))
    CL Item
    Tumor registry (Tumor registry)
    CL Item
    Other (specify) (Other (specify))

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