0 Bedömningar
ID

42675

Beskrivning

ODM derived from http://clinicaltrials.gov/show/NCT00606723

Länk

http://clinicaltrials.gov/show/NCT00606723

Nyckelord

Versioner (2)
  1. 2013-12-06 2013-12-06 - Martin Dugas
  2. 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 DRKS00002025 NCT00606723 Acute Myeloid Leukemia (AML)

    Tysk Engelsk

    Eligibility

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

    Einschlusskriterien

    Alias
    UMLS CUI 2011AA
    CL425202
    Alter bis zu 21 Jahre
    Beskrivning

    age up to 21 Years

    Datatyp

    boolean

    Alias
    UMLS CUI 2011AA
    C0001779
    SNOMED CT 2011_0131
    397669002
    Children, adolescents and young adults aged 0-21 years, male and female
    Beskrivning

    Children, adolescents and young adults aged 0-21 years, male and female

    Datatyp

    boolean

    Alias
    UMLS CUI 2011AA
    C0008059
    SNOMED CT 2011_0131
    67822003
    HL7 V3 2006_05
    CHILD
    UMLS CUI 2011AA
    C0205653
    SNOMED CT 2011_0131
    133937008
    UMLS CUI 2011AA
    C0238598
    UMLS CUI 2011AA
    C0001779
    SNOMED CT 2011_0131
    397669002
    UMLS CUI 2011AA
    C0086582
    SNOMED CT 2011_0131
    248153007
    HL7 V3 2006_05
    M
    UMLS CUI 2011AA
    C0086287
    SNOMED CT 2011_0131
    248152002
    HL7 V3 2006_05
    F
    Patients suffering from refractory de novo AML
    Beskrivning

    Patients suffering from refractory de novo AML

    Datatyp

    boolean

    Alias
    UMLS CUI 2011AA
    C0205269
    SNOMED CT 2011_0131
    20646008
    UMLS CUI 2011AA
    C1515568
    UMLS CUI 2011AA
    C0023467
    SNOMED CT 2011_0131
    91861009
    MedDRA 14.1
    10000880
    ICD-10-CM Version 2010
    C92.0
    ICD-9-CM Version 2011
    205.0
    UMLS CUI 2011AA
    C0011900
    SNOMED CT 2011_0131
    439401001
    LOINC Version 232
    MTHU008876
    Patients with relapsed AML
    Beskrivning

    Patients with relapsed AML

    Datatyp

    boolean

    Alias
    UMLS CUI 2011AA
    C0035020
    SNOMED CT 2011_0131
    263855007
    UMLS CUI 2011AA
    C0023467
    SNOMED CT 2011_0131
    91861009
    MedDRA 14.1
    10000880
    ICD-10-CM Version 2010
    C92.0
    ICD-9-CM Version 2011
    205.0
    UMLS CUI 2011AA
    C0278780
    sekundäre AML
    Beskrivning

    Patients with secondary AML

    Datatyp

    boolean

    Alias
    UMLS CUI 2011AA
    C0280449
    Ausschlusskriterien
    Beskrivning

    Ausschlusskriterien

    Alias
    UMLS CUI 2011AA
    CL425201
    Severely impaired functional performance
    Beskrivning

    Severely impaired functional performance

    Datatyp

    boolean

    Alias
    UMLS CUI 2011AA
    C0205082
    SNOMED CT 2011_0131
    24484000
    UMLS CUI 2011AA
    C0221099
    SNOMED CT 2011_0131
    260379002
    UMLS CUI 2011AA
    C0424866
    SNOMED CT 2011_0131
    248536006
    Severe renal impairment
    Beskrivning

    Severe renal impairment

    Datatyp

    boolean

    Alias
    UMLS CUI 2011AA
    C0205082
    SNOMED CT 2011_0131
    24484000
    UMLS CUI 2011AA
    C1565489
    SNOMED CT 2011_0131
    236423003
    MedDRA 14.1
    10062237
    Schwangerschaft
    Beskrivning

    Pregnancy

    Datatyp

    boolean

    Alias
    UMLS CUI 2011AA
    C0032961
    SNOMED CT 2011_0131
    289908002
    MedDRA 14.1
    10036556
    LOINC Version 232
    MTHU035048
    Current participation in another clinical trial
    Beskrivning

    Current participation in another clinical trial

    Datatyp

    boolean

    Alias
    UMLS CUI 2011AA
    C0521116
    SNOMED CT 2011_0131
    15240007
    UMLS CUI 2011AA
    C0679823
    HL7 V3 2006_05
    PART
    UMLS CUI 2011AA
    C0205394
    SNOMED CT 2011_0131
    74964007
    UMLS CUI 2011AA
    C0008976
    SNOMED CT 2011_0131
    110465008
    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 up to 21 Years
    Item
    Alter bis zu 21 Jahre
    boolean
    C0001779 (UMLS CUI 2011AA)
    397669002 (SNOMED CT 2011_0131)
    Children, adolescents and young adults aged 0-21 years, male and female
    Item
    Children, adolescents and young adults aged 0-21 years, male and female
    boolean
    C0008059 (UMLS CUI 2011AA)
    67822003 (SNOMED CT 2011_0131)
    CHILD (HL7 V3 2006_05)
    C0205653 (UMLS CUI 2011AA)
    133937008 (SNOMED CT 2011_0131)
    C0238598 (UMLS CUI 2011AA)
    C0001779 (UMLS CUI 2011AA)
    397669002 (SNOMED CT 2011_0131)
    C0086582 (UMLS CUI 2011AA)
    248153007 (SNOMED CT 2011_0131)
    M (HL7 V3 2006_05)
    C0086287 (UMLS CUI 2011AA)
    248152002 (SNOMED CT 2011_0131)
    F (HL7 V3 2006_05)
    Patients suffering from refractory de novo AML
    Item
    Patients suffering from refractory de novo AML
    boolean
    C0205269 (UMLS CUI 2011AA)
    20646008 (SNOMED CT 2011_0131)
    C1515568 (UMLS CUI 2011AA)
    C0023467 (UMLS CUI 2011AA)
    91861009 (SNOMED CT 2011_0131)
    10000880 (MedDRA 14.1)
    C92.0 (ICD-10-CM Version 2010)
    205.0 (ICD-9-CM Version 2011)
    C0011900 (UMLS CUI 2011AA)
    439401001 (SNOMED CT 2011_0131)
    MTHU008876 (LOINC Version 232)
    Patients with relapsed AML
    Item
    Patients with relapsed AML
    boolean
    C0035020 (UMLS CUI 2011AA)
    263855007 (SNOMED CT 2011_0131)
    C0023467 (UMLS CUI 2011AA)
    91861009 (SNOMED CT 2011_0131)
    10000880 (MedDRA 14.1)
    C92.0 (ICD-10-CM Version 2010)
    205.0 (ICD-9-CM Version 2011)
    C0278780 (UMLS CUI 2011AA)
    Patients with secondary AML
    Item
    sekundäre AML
    boolean
    C0280449 (UMLS CUI 2011AA)
    Item Group
    Ausschlusskriterien
    CL425201 (UMLS CUI 2011AA)
    Severely impaired functional performance
    Item
    Severely impaired functional performance
    boolean
    C0205082 (UMLS CUI 2011AA)
    24484000 (SNOMED CT 2011_0131)
    C0221099 (UMLS CUI 2011AA)
    260379002 (SNOMED CT 2011_0131)
    C0424866 (UMLS CUI 2011AA)
    248536006 (SNOMED CT 2011_0131)
    Severe renal impairment
    Item
    Severe renal impairment
    boolean
    C0205082 (UMLS CUI 2011AA)
    24484000 (SNOMED CT 2011_0131)
    C1565489 (UMLS CUI 2011AA)
    236423003 (SNOMED CT 2011_0131)
    10062237 (MedDRA 14.1)
    Pregnancy
    Item
    Schwangerschaft
    boolean
    C0032961 (UMLS CUI 2011AA)
    289908002 (SNOMED CT 2011_0131)
    10036556 (MedDRA 14.1)
    MTHU035048 (LOINC Version 232)
    Current participation in another clinical trial
    Item
    Current participation in another clinical trial
    boolean
    C0521116 (UMLS CUI 2011AA)
    15240007 (SNOMED CT 2011_0131)
    C0679823 (UMLS CUI 2011AA)
    PART (HL7 V3 2006_05)
    C0205394 (UMLS CUI 2011AA)
    74964007 (SNOMED CT 2011_0131)
    C0008976 (UMLS CUI 2011AA)
    110465008 (SNOMED CT 2011_0131)
    Tillbaka till toppen 

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