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ID

42687

Beskrivning

ODM derived from http://clinicaltrials.gov/show/NCT01207388

Länk

http://clinicaltrials.gov/show/NCT01207388

Nyckelord

Versioner (3)
  1. 2013-12-06 2013-12-06 - Martin Dugas
  2. 2013-12-06 2013-12-06 - Martin Dugas
  3. 2021-09-17 2021-09-17 -
Uppladdad den

17 september 2021

DOI

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Creative Commons BY 4.0
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    Eligibility DRKS00005163 NCT01134939 HIV Infections

    Tysk Engelsk

    Eligibility

    1 Formulär  
    1. StudyEvent: Eligibility
      1. Eligibility
    Einschlusskriterien
    Beskrivning

    Einschlusskriterien

    Alias
    UMLS CUI 2011AA
    CL425202
    Alter mindestens 18 Jahre
    Beskrivning

    age at least 18 Years

    Datatyp

    boolean

    Alias
    UMLS CUI 2011AA
    C0001779
    SNOMED CT 2011_0131
    397669002
    Patients with B-precursor ALL in complete hematological remission after at least 3 intense chemotherapy blocks
    Beskrivning

    Patients with B-precursor ALL in complete hematological remission after at least 3 intense chemotherapy blocks

    Datatyp

    boolean

    Alias
    UMLS CUI 2011AA
    C1292769
    SNOMED CT 2011_0131
    128823009
    MedDRA 14.1
    10003890
    UMLS CUI 2011AA
    C0011900
    SNOMED CT 2011_0131
    439401001
    LOINC Version 232
    MTHU008876
    UMLS CUI 2011AA
    C0205488
    SNOMED CT 2011_0131
    57407000
    UMLS CUI 2011AA
    C0677874
    SNOMED CT 2011_0131
    103338009
    UMLS CUI 2011AA
    C0522510
    SNOMED CT 2011_0131
    103370009
    UMLS CUI 2011AA
    C1302181
    SNOMED CT 2011_0131
    399042005
    Presence of minimal residual disease at a level of >=10-3
    Beskrivning

    Presence of minimal residual disease at a level of >=10-3

    Datatyp

    boolean

    Alias
    UMLS CUI 2011AA
    C0150312
    SNOMED CT 2011_0131
    52101004
    UMLS CUI 2011AA
    C0242596
    UMLS CUI 2011AA
    C0456079
    SNOMED CT 2011_0131
    276625007
    Availability of bone marrow specimen from primary diagnosis for clone-specific MRD assessment
    Beskrivning

    Availability of bone marrow specimen from primary diagnosis for clone-specific MRD assessment

    Datatyp

    boolean

    Alias
    UMLS CUI 2011AA
    C0470187
    SNOMED CT 2011_0131
    103328004
    UMLS CUI 2011AA
    C0438737
    SNOMED CT 2011_0131
    119359002
    UMLS CUI 2011AA
    C0801658
    LOINC Version 232
    18630-4
    UMLS CUI 2011AA
    C1522642
    UMLS CUI 2011AA
    C1552740
    HL7 V3 2006_05
    INSTANCE
    UMLS CUI 2011AA
    C0242596
    UMLS CUI 2011AA
    C1516048
    Negative HIV test, negative hepatitis B (HbsAg) test and hepatitis C virus (anti-HCV) test
    Beskrivning

    Negative HIV test, negative hepatitis B (HbsAg) test and hepatitis C virus (anti-HCV) test

    Datatyp

    boolean

    Alias
    UMLS CUI 2011AA
    C0481430
    SNOMED CT 2011_0131
    143223008
    MedDRA 14.1
    10020179
    UMLS CUI 2011AA
    C1611173
    MedDRA 14.1
    10065002
    UMLS CUI 2011AA
    C0919711
    SNOMED CT 2011_0131
    406010001
    MedDRA 14.1
    10050542
    UMLS CUI 2011AA
    C1619717
    MedDRA 14.1
    10065001
    UMLS CUI 2011AA
    C0166049
    SNOMED CT 2011_0131
    72165005
    LOINC Version 232
    MTHU004551
    UMLS CUI 2011AA
    C0392366
    SNOMED CT 2011_0131
    272393004
    Negative pregnancy test in women of childbearing potential
    Beskrivning

    Negative pregnancy test in women of childbearing potential

    Datatyp

    boolean

    Alias
    UMLS CUI 2011AA
    C0427780
    SNOMED CT 2011_0131
    250425007
    MedDRA 14.1
    10036574
    UMLS CUI 2011AA
    C0043210
    SNOMED CT 2011_0131
    224526002
    UMLS CUI 2011AA
    C1148523
    UMLS CUI 2011AA
    C0237399
    ECOG performance status 0 or 1
    Beskrivning

    ECOG performance status 0 or 1

    Datatyp

    boolean

    Alias
    UMLS CUI 2011AA
    C1828078
    SNOMED CT 2011_0131
    425389002
    UMLS CUI 2011AA
    C1827388
    SNOMED CT 2011_0131
    422512005
    Ausschlusskriterien
    Beskrivning

    Ausschlusskriterien

    Alias
    UMLS CUI 2011AA
    CL425201
    Presence of circulating blasts or current extra-medullary involvement by ALL
    Beskrivning

    Presence of circulating blasts or current extra-medullary involvement by ALL

    Datatyp

    boolean

    Alias
    UMLS CUI 2011AA
    C0150312
    SNOMED CT 2011_0131
    52101004
    UMLS CUI 2011AA
    C0175630
    SNOMED CT 2011_0131
    65929005
    UMLS CUI 2011AA
    C0368761
    SNOMED CT 2011_0131
    312256009
    LOINC Version 232
    MTHU005201
    UMLS CUI 2011AA
    C1517060
    UMLS CUI 2011AA
    C1314939
    SNOMED CT 2011_0131
    248448006
    UMLS CUI 2011AA
    C0023449
    SNOMED CT 2011_0131
    91857003, 128822004
    MedDRA 14.1
    10060390
    ICD-10-CM Version 2010
    C91.0
    ICD-9-CM Version 2011
    204.0
    History of relevant CNS pathology or current CNS pathology
    Beskrivning

    History of relevant CNS pathology or current CNS pathology

    Datatyp

    boolean

    Alias
    UMLS CUI 2011AA
    CL421546
    SNOMED CT 2011_0131
    392521001
    UMLS CUI 2011AA
    C2347946
    UMLS CUI 2011AA
    C0521116
    SNOMED CT 2011_0131
    15240007
    UMLS CUI 2011AA
    C1269563
    SNOMED CT 2011_0131
    278199004
    UMLS CUI 2011AA
    C0677042
    Prior allogeneic HSCT
    Beskrivning

    Prior allogeneic HSCT

    Datatyp

    boolean

    Alias
    UMLS CUI 2011AA
    C0332152
    SNOMED CT 2011_0131
    288556008
    UMLS CUI 2011AA
    C2242529
    MedDRA 14.1
    10067862
    Eligibility for treatment with TKIs
    Beskrivning

    Eligibility for treatment with TKIs

    Datatyp

    boolean

    Alias
    UMLS CUI 2011AA
    C0013893
    UMLS CUI 2011AA
    C0039798
    UMLS CUI 2011AA
    C1268567
    SNOMED CT 2011_0131
    372917005
    Systemic cancer chemotherapy within 2 weeks prior to study treatment
    Beskrivning

    Systemic cancer chemotherapy within 2 weeks prior to study treatment

    Datatyp

    boolean

    Alias
    UMLS CUI 2011AA
    C1883256
    UMLS CUI 2011AA
    C0006826
    SNOMED CT 2011_0131
    363346000
    MedDRA 14.1
    10028997
    LOINC Version 232
    MTHU010328
    ICD-10-CM Version 2010
    C00-C96
    UMLS CUI 2011AA
    C0205448
    SNOMED CT 2011_0131
    19338005
    UMLS CUI 2011AA
    C0439230
    SNOMED CT 2011_0131
    258705008
    HL7 V3 2006_05
    WK
    UMLS CUI 2011AA
    C0332152
    SNOMED CT 2011_0131
    288556008
    UMLS CUI 2011AA
    C0008976
    SNOMED CT 2011_0131
    110465008
    UMLS CUI 2011AA
    C0039798
    Therapy with monoclonal antibodies (rituximab, alemtuzumab) within 4 weeks prior to study treatment
    Beskrivning

    Therapy with monoclonal antibodies (rituximab, alemtuzumab) within 4 weeks prior to study treatment

    Datatyp

    boolean

    Alias
    UMLS CUI 2011AA
    C0039798
    UMLS CUI 2011AA
    C0003250
    SNOMED CT 2011_0131
    49616005
    UMLS CUI 2011AA
    C0732355
    SNOMED CT 2011_0131
    386919002
    UMLS CUI 2011AA
    C0383429
    SNOMED CT 2011_0131
    391864003
    Previous treatment with blinatumomab
    Beskrivning

    Previous treatment with blinatumomab

    Datatyp

    boolean

    Alias
    UMLS CUI 2011AA
    C1514463
    UMLS CUI 2011AA
    C3853839
    Tillbaka till toppen

    Similar models

    Eligibility

    1 Formulär
    1. StudyEvent: Eligibility
      1. Eligibility
    Name
    Typ
    Description | Question | Decode (Coded Value)
    Datatyp
    Alias
    Item Group
    Einschlusskriterien
    CL425202 (UMLS CUI 2011AA)
    age at least 18 Years
    Item
    Alter mindestens 18 Jahre
    boolean
    C0001779 (UMLS CUI 2011AA)
    397669002 (SNOMED CT 2011_0131)
    Patients with B-precursor ALL in complete hematological remission after at least 3 intense chemotherapy blocks
    Item
    Patients with B-precursor ALL in complete hematological remission after at least 3 intense chemotherapy blocks
    boolean
    C1292769 (UMLS CUI 2011AA)
    128823009 (SNOMED CT 2011_0131)
    10003890 (MedDRA 14.1)
    C0011900 (UMLS CUI 2011AA)
    439401001 (SNOMED CT 2011_0131)
    MTHU008876 (LOINC Version 232)
    C0205488 (UMLS CUI 2011AA)
    57407000 (SNOMED CT 2011_0131)
    C0677874 (UMLS CUI 2011AA)
    103338009 (SNOMED CT 2011_0131)
    C0522510 (UMLS CUI 2011AA)
    103370009 (SNOMED CT 2011_0131)
    C1302181 (UMLS CUI 2011AA)
    399042005 (SNOMED CT 2011_0131)
    Presence of minimal residual disease at a level of >=10-3
    Item
    Presence of minimal residual disease at a level of >=10-3
    boolean
    C0150312 (UMLS CUI 2011AA)
    52101004 (SNOMED CT 2011_0131)
    C0242596 (UMLS CUI 2011AA)
    C0456079 (UMLS CUI 2011AA)
    276625007 (SNOMED CT 2011_0131)
    Availability of bone marrow specimen from primary diagnosis for clone-specific MRD assessment
    Item
    Availability of bone marrow specimen from primary diagnosis for clone-specific MRD assessment
    boolean
    C0470187 (UMLS CUI 2011AA)
    103328004 (SNOMED CT 2011_0131)
    C0438737 (UMLS CUI 2011AA)
    119359002 (SNOMED CT 2011_0131)
    C0801658 (UMLS CUI 2011AA)
    18630-4 (LOINC Version 232)
    C1522642 (UMLS CUI 2011AA)
    C1552740 (UMLS CUI 2011AA)
    INSTANCE (HL7 V3 2006_05)
    C0242596 (UMLS CUI 2011AA)
    C1516048 (UMLS CUI 2011AA)
    Negative HIV test, negative hepatitis B (HbsAg) test and hepatitis C virus (anti-HCV) test
    Item
    Negative HIV test, negative hepatitis B (HbsAg) test and hepatitis C virus (anti-HCV) test
    boolean
    C0481430 (UMLS CUI 2011AA)
    143223008 (SNOMED CT 2011_0131)
    10020179 (MedDRA 14.1)
    C1611173 (UMLS CUI 2011AA)
    10065002 (MedDRA 14.1)
    C0919711 (UMLS CUI 2011AA)
    406010001 (SNOMED CT 2011_0131)
    10050542 (MedDRA 14.1)
    C1619717 (UMLS CUI 2011AA)
    10065001 (MedDRA 14.1)
    C0166049 (UMLS CUI 2011AA)
    72165005 (SNOMED CT 2011_0131)
    MTHU004551 (LOINC Version 232)
    C0392366 (UMLS CUI 2011AA)
    272393004 (SNOMED CT 2011_0131)
    Negative pregnancy test in women of childbearing potential
    Item
    Negative pregnancy test in women of childbearing potential
    boolean
    C0427780 (UMLS CUI 2011AA)
    250425007 (SNOMED CT 2011_0131)
    10036574 (MedDRA 14.1)
    C0043210 (UMLS CUI 2011AA)
    224526002 (SNOMED CT 2011_0131)
    C1148523 (UMLS CUI 2011AA)
    C0237399 (UMLS CUI 2011AA)
    ECOG performance status 0 or 1
    Item
    ECOG performance status 0 or 1
    boolean
    C1828078 (UMLS CUI 2011AA)
    425389002 (SNOMED CT 2011_0131)
    C1827388 (UMLS CUI 2011AA)
    422512005 (SNOMED CT 2011_0131)
    Item Group
    Ausschlusskriterien
    CL425201 (UMLS CUI 2011AA)
    Presence of circulating blasts or current extra-medullary involvement by ALL
    Item
    Presence of circulating blasts or current extra-medullary involvement by ALL
    boolean
    C0150312 (UMLS CUI 2011AA)
    52101004 (SNOMED CT 2011_0131)
    C0175630 (UMLS CUI 2011AA)
    65929005 (SNOMED CT 2011_0131)
    C0368761 (UMLS CUI 2011AA)
    312256009 (SNOMED CT 2011_0131)
    MTHU005201 (LOINC Version 232)
    C1517060 (UMLS CUI 2011AA)
    C1314939 (UMLS CUI 2011AA)
    248448006 (SNOMED CT 2011_0131)
    C0023449 (UMLS CUI 2011AA)
    91857003, 128822004 (SNOMED CT 2011_0131)
    10060390 (MedDRA 14.1)
    C91.0 (ICD-10-CM Version 2010)
    204.0 (ICD-9-CM Version 2011)
    History of relevant CNS pathology or current CNS pathology
    Item
    History of relevant CNS pathology or current CNS pathology
    boolean
    CL421546 (UMLS CUI 2011AA)
    392521001 (SNOMED CT 2011_0131)
    C2347946 (UMLS CUI 2011AA)
    C0521116 (UMLS CUI 2011AA)
    15240007 (SNOMED CT 2011_0131)
    C1269563 (UMLS CUI 2011AA)
    278199004 (SNOMED CT 2011_0131)
    C0677042 (UMLS CUI 2011AA)
    Prior allogeneic HSCT
    Item
    Prior allogeneic HSCT
    boolean
    C0332152 (UMLS CUI 2011AA)
    288556008 (SNOMED CT 2011_0131)
    C2242529 (UMLS CUI 2011AA)
    10067862 (MedDRA 14.1)
    Eligibility for treatment with TKIs
    Item
    Eligibility for treatment with TKIs
    boolean
    C0013893 (UMLS CUI 2011AA)
    C0039798 (UMLS CUI 2011AA)
    C1268567 (UMLS CUI 2011AA)
    372917005 (SNOMED CT 2011_0131)
    Systemic cancer chemotherapy within 2 weeks prior to study treatment
    Item
    Systemic cancer chemotherapy within 2 weeks prior to study treatment
    boolean
    C1883256 (UMLS CUI 2011AA)
    C0006826 (UMLS CUI 2011AA)
    363346000 (SNOMED CT 2011_0131)
    10028997 (MedDRA 14.1)
    MTHU010328 (LOINC Version 232)
    C00-C96 (ICD-10-CM Version 2010)
    C0205448 (UMLS CUI 2011AA)
    19338005 (SNOMED CT 2011_0131)
    C0439230 (UMLS CUI 2011AA)
    258705008 (SNOMED CT 2011_0131)
    WK (HL7 V3 2006_05)
    C0332152 (UMLS CUI 2011AA)
    288556008 (SNOMED CT 2011_0131)
    C0008976 (UMLS CUI 2011AA)
    110465008 (SNOMED CT 2011_0131)
    C0039798 (UMLS CUI 2011AA)
    Therapy with monoclonal antibodies (rituximab, alemtuzumab) within 4 weeks prior to study treatment
    Item
    Therapy with monoclonal antibodies (rituximab, alemtuzumab) within 4 weeks prior to study treatment
    boolean
    C0039798 (UMLS CUI 2011AA)
    C0003250 (UMLS CUI 2011AA)
    49616005 (SNOMED CT 2011_0131)
    C0732355 (UMLS CUI 2011AA)
    386919002 (SNOMED CT 2011_0131)
    C0383429 (UMLS CUI 2011AA)
    391864003 (SNOMED CT 2011_0131)
    Previous treatment with blinatumomab
    Item
    Previous treatment with blinatumomab
    boolean
    C1514463 (UMLS CUI 2011AA)
    C3853839 (UMLS CUI 2011AA)
    Tillbaka till toppen 

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