0 Evaluaciones
ID

31176

Descripción

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

Palabras clave

Versiones (1)
  1. 25/7/18 25/7/18 -
Titular de derechos de autor

see clinicaltrials.gov

Subido en

25 de julio de 2018

DOI

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Licencia

Creative Commons BY 4.0
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    Iodine 131 B1 Antibody for B-Cell Lymphomas NCT00950755

    Inglés

    Notification of Patient Death

    1 formularios  
    Administrative Data
    Descripción

    Administrative Data

    Alias
    UMLS CUI-1
    C1320722 (Administrative documentation)
    SNOMED
    405624007
    Site Number
    Descripción

    Site number

    Tipo de datos

    text

    Alias
    UMLS CUI [1,1]
    C0018704 (Health care facility)
    SNOMED
    257622000
    LOINC
    LA30302-6
    UMLS CUI [1,2]
    C0600091 (Identifier)
    SNOMED
    118522005
    LOINC
    LP31795-5
    Patient Number
    Descripción

    Patient Number

    Tipo de datos

    text

    Alias
    UMLS CUI [1]
    C1830427 (undefined)
    Patient Initials
    Descripción

    Patient Initials

    Tipo de datos

    text

    Alias
    UMLS CUI [1]
    C2986440 (Person Initials)
    Patient Death
    Descripción

    Patient Death

    Alias
    UMLS CUI-1
    C0011065 (Cessation of life)
    SNOMED
    419620001
    Date of death
    Descripción

    Date of death

    Tipo de datos

    date

    Alias
    UMLS CUI [1]
    C1148348 (Date of death)
    SNOMED
    399753006
    LOINC
    MTHU014693
    Cause of death (check one)
    Descripción

    Cause of death

    Tipo de datos

    text

    Alias
    UMLS CUI [1]
    C0007465 (Cause of Death)
    SNOMED
    16100001
    LOINC
    LA10595-9
    If cause of death was related to complications of treatment, please describe or reference forms on which information was recorded.
    Descripción

    Complications of treatment

    Tipo de datos

    text

    Alias
    UMLS CUI [1,1]
    C0087111 (Therapeutic procedure)
    SNOMED
    277132007
    LOINC
    LP21090-3
    UMLS CUI [1,2]
    C0009566 (Complication)
    SNOMED
    116223007
    Relations of study drug to patients death
    Descripción

    Study drug relation to death

    Tipo de datos

    text

    Alias
    UMLS CUI [1,1]
    C0011065 (Cessation of life)
    SNOMED
    419620001
    UMLS CUI [1,2]
    C0304229 (Experimental drug)
    Source of information concerning death of patient (check all that apply)
    Descripción

    Patient death; Source of Information

    Tipo de datos

    text

    Alias
    UMLS CUI [1,1]
    C0011065 (Cessation of life)
    SNOMED
    419620001
    UMLS CUI [1,2]
    C1955348 (Patient Information)
    UMLS CUI [1,3]
    C0449416 (Source)
    SNOMED
    260753009
    LOINC
    LP21212-3
    Volver a la parte superior de la página

    Similar models

    Notification of Patient Death

    1 formularios
    Name
    Tipo
    Description | Question | Decode (Coded Value)
    Tipo de datos
    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])
    Cause of death
    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])
    Study drug relation
    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])
    Patient death; Source of Information
    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))
    Volver a la parte superior de la página 

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