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ID

4763

Description

Functional and Clinical Long-Term Outcome of Ewing Sarcoma Treatment see http://clinicaltrials.gov/show/NCT00824083

Lien

http://clinicaltrials.gov/show/NCT00824083

Mots-clés

Versions (2)
  1. 25/07/2013 25/07/2013 - Martin Dugas
  2. 27/03/2014 27/03/2014 - Martin Dugas
Téléchargé le

27 mars 2014

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0
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    Eligibility DRKS00003588 NCT00824083 Sarcoma, Ewing's

    Allemand Anglais

    Eligibility Ewing Sarcoma NCT00824083

    1 Formulaires  
    Einschlusskriterien
    Description

    Einschlusskriterien

    Alias
    UMLS CUI 2011AA
    CL425202 (undefined)
    Alter 6 bis 60 Jahre
    Description

    age

    Type de données

    boolean

    Alias
    SNOMED CT 2011_0131
    397669002 (undefined)
    UMLS CUI-1
    C0001779 (Age)
    SNOMED
    424144002
    LOINC
    LP28815-6
    CESS81/CESS86/EICESS92/EURO-E.W.I.N.G.99 trials participants of the German Society of Pediatric Hematology and Oncology (GPOH)
    Description

    Trial participant (Ewing trials GPOH)

    Type de données

    boolean

    Alias
    SNOMED CT 2011_0131
    414152003 (undefined)
    HL7 V3 2006_05
    2108-9 (undefined)
    SNOMED CT 2011_0131
    76909002 (undefined)
    MedDRA 14.1
    10015560 (undefined)
    SNOMED CT 2011_0131
    439401001 (undefined)
    LOINC Version 232
    MTHU008876 (undefined)
    SNOMED CT 2011_0131
    110465008 (undefined)
    SNOMED CT 2011_0131
    418652005 (undefined)
    SNOMED CT 2011_0131
    418002000 (undefined)
    UMLS CUI-1
    C0553580 (Ewings sarcoma)
    SNOMED
    76909002
    UMLS CUI-2
    C0008976 (Clinical Trials)
    SNOMED
    110465008
    LOINC
    LP231796-6
    UMLS CUI-3
    C0679646 (Participant)
    Ausschlusskriterien
    Description

    Ausschlusskriterien

    Alias
    UMLS CUI-1
    C0680251 (Exclusion Criteria)
    no complete remission (CR)
    Description

    no complete remission (CR)

    Type de données

    boolean

    Alias
    UMLS CUI 2011AA
    C1518422 (Negation)
    LOINC
    LA21291-2
    UMLS CUI 2011AA
    C0677874 (In complete remission)
    SNOMED
    103338009
    SNOMED CT 2011_0131
    103338009 (undefined)
    any kind of paralysis
    Description

    Paralysis

    Type de données

    boolean

    Alias
    SNOMED CT 2011_0131
    44695005 (undefined)
    MedDRA 14.1
    10033799 (undefined)
    ICD-9-CM Version 2011
    344.9 (undefined)
    UMLS CUI-1
    C0522224 (Paralysed)
    SNOMED
    44695005
    <5y after diagnosis
    Description

    Time after diagnosis

    Type de données

    boolean

    Alias
    SNOMED CT 2011_0131
    276139006 (undefined)
    HL7 V3 2006_05
    LT (undefined)
    SNOMED CT 2011_0131
    34001005 (undefined)
    SNOMED CT 2011_0131
    258707000 (undefined)
    HL7 V3 2006_05
    Y (undefined)
    SNOMED CT 2011_0131
    237679004 (undefined)
    SNOMED CT 2011_0131
    439401001 (undefined)
    LOINC Version 232
    MTHU008876 (undefined)
    UMLS CUI-1
    C0231290 (Status post)
    SNOMED
    237679004
    UMLS CUI-2
    C0011900 (Diagnosis)
    SNOMED
    439401001
    LOINC
    LP30831-9
    Retour au début de la page

    Similar models

    Eligibility Ewing Sarcoma NCT00824083

    1 Formulaires
    Name
    Type
    Description | Question | Decode (Coded Value)
    Type de données
    Alias
    Item Group
    Einschlusskriterien
    CL425202 (UMLS CUI 2011AA)
    age
    Item
    Alter 6 bis 60 Jahre
    boolean
    397669002 (SNOMED CT 2011_0131)
    C0001779 (UMLS CUI-1)
    Trial participant (Ewing trials GPOH)
    Item
    CESS81/CESS86/EICESS92/EURO-E.W.I.N.G.99 trials participants of the German Society of Pediatric Hematology and Oncology (GPOH)
    boolean
    414152003 (SNOMED CT 2011_0131)
    2108-9 (HL7 V3 2006_05)
    76909002 (SNOMED CT 2011_0131)
    10015560 (MedDRA 14.1)
    439401001 (SNOMED CT 2011_0131)
    MTHU008876 (LOINC Version 232)
    110465008 (SNOMED CT 2011_0131)
    418652005 (SNOMED CT 2011_0131)
    418002000 (SNOMED CT 2011_0131)
    C0553580 (UMLS CUI-1)
    C0008976 (UMLS CUI-2)
    C0679646 (UMLS CUI-3)
    Item Group
    Ausschlusskriterien
    C0680251 (UMLS CUI-1)
    no complete remission (CR)
    Item
    no complete remission (CR)
    boolean
    C1518422 (UMLS CUI 2011AA)
    C0677874 (UMLS CUI 2011AA)
    103338009 (SNOMED CT 2011_0131)
    Paralysis
    Item
    any kind of paralysis
    boolean
    44695005 (SNOMED CT 2011_0131)
    10033799 (MedDRA 14.1)
    344.9 (ICD-9-CM Version 2011)
    C0522224 (UMLS CUI-1)
    Time after diagnosis
    Item
    <5y after diagnosis
    boolean
    276139006 (SNOMED CT 2011_0131)
    LT (HL7 V3 2006_05)
    34001005 (SNOMED CT 2011_0131)
    258707000 (SNOMED CT 2011_0131)
    Y (HL7 V3 2006_05)
    237679004 (SNOMED CT 2011_0131)
    439401001 (SNOMED CT 2011_0131)
    MTHU008876 (LOINC Version 232)
    C0231290 (UMLS CUI-1)
    C0011900 (UMLS CUI-2)
    Retour au début de la page 

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