0 Beoordelingen
ID

3853

Beschrijving

ODM derived from http://clinicaltrials.gov/show/NCT01423747

Link

http://clinicaltrials.gov/show/NCT01423747

Trefwoorden

Versies (2)
  1. 17-04-13 17-04-13 - Martin Dugas
  2. 20-04-14 20-04-14 - Julian Varghese
Geüploaded op

17 april 2013

DOI

Voor een aanvraag inloggen.

Licentie

Creative Commons BY-NC 3.0 Legacy
Model Commentaren :

Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.

Terug naar het model Commentaren
Itemgroep Commentaren voor :

Item Commentaren voor :

  • Nieuwste
  • Oudste
  • Populair
  • Nieuwste
    • Nieuwste
    • Oudste
    • Populair

    Geen commentaren

    U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.

    Eligibility NCT01423747 Lymphoblastic Leukemia, Acute, Childhood

    Duits Engels

    Eligibility

    1 Formulieren  
    1. StudyEvent: Eligibility
      1. Eligibility
    Einschlusskriterien
    Beschrijving

    Einschlusskriterien

    Alter 3 Monate bis 18 Jahre
    Beschrijving

    age 3 Months to 18 Years

    Datatype

    boolean

    Alias
    UMLS CUI 2011AA
    C0001779
    SNOMED CT 2011_0131
    397669002
    Lymphoblastic Leukemia, Acute, Childhood
    Beschrijving

    Lymphoblastic Leukemia, Acute, Childhood

    Datatype

    boolean

    Alias
    UMLS CUI 2011AA
    C0023452
    UMLS CUI 2011AA
    C0011900
    SNOMED CT 2011_0131
    439401001
    LOINC Version 232
    MTHU008876
    age at time of initial diagnosis or relapse diagnosis, respectively under or equal 18 years
    Beschrijving

    age at time of initial diagnosis or relapse diagnosis, respectively under or equal 18 years

    Datatype

    boolean

    Alias
    UMLS CUI 2011AA
    C0205265
    SNOMED CT 2011_0131
    884001
    UMLS CUI 2011AA
    C0277556
    SNOMED CT 2011_0131
    58184002
    UMLS CUI 2011AA
    C0011900
    SNOMED CT 2011_0131
    439401001
    LOINC Version 232
    MTHU008876
    indication for allogeneic HSCT
    Beschrijving

    indication for allogeneic HSCT

    Datatype

    boolean

    Alias
    UMLS CUI 2011AA
    CL335836
    UMLS CUI 2011AA
    C2242529
    MedDRA 14.1
    10067862
    complete remission before HSCT
    Beschrijving

    complete remission before HSCT

    Datatype

    boolean

    Alias
    UMLS CUI 2011AA
    C0677874
    SNOMED CT 2011_0131
    103338009
    UMLS CUI 2011AA
    C0332152
    SNOMED CT 2011_0131
    288556008
    UMLS CUI 2011AA
    C2242529
    MedDRA 14.1
    10067862
    written consent of the parents (legal guardian) and, if necessary, the minor patient via Informed Consent Form
    Beschrijving

    written consent of the parents (legal guardian) and, if necessary, the minor patient via Informed Consent Form

    Datatype

    boolean

    Alias
    UMLS CUI 2011AA
    C1576874
    HL7 V3 2006_05
    WRITTEN
    UMLS CUI 2011AA
    C0009797
    UMLS CUI 2011AA
    C0030551
    SNOMED CT 2011_0131
    40683002
    HL7 V3 2006_05
    PARNT
    UMLS CUI 2011AA
    C0023226
    SNOMED CT 2011_0131
    58626002
    LOINC Version 232
    MTHU020628
    UMLS CUI 2011AA
    C0026193
    SNOMED CT 2011_0131
    410599005
    UMLS CUI 2011AA
    C0030705
    SNOMED CT 2011_0131
    116154003
    nicht schwanger
    Beschrijving

    no pregnancy

    Datatype

    boolean

    Alias
    UMLS CUI 2011AA
    C0232973
    SNOMED CT 2011_0131
    60001007
    no secondary malignancy
    Beschrijving

    no secondary malignancy

    Datatype

    boolean

    Alias
    UMLS CUI 2011AA
    C0332197
    SNOMED CT 2011_0131
    2667000
    UMLS CUI 2011AA
    C0027627
    SNOMED CT 2011_0131
    128462008
    no previous HSCT
    Beschrijving

    no previous HSCT

    Datatype

    boolean

    Alias
    UMLS CUI 2011AA
    C0332197
    SNOMED CT 2011_0131
    2667000
    UMLS CUI 2011AA
    C0205156
    SNOMED CT 2011_0131
    9130008
    UMLS CUI 2011AA
    C2242529
    MedDRA 14.1
    10067862
    HSCT is performed in a study participating centre.
    Beschrijving

    HSCT is performed in a study participating centre.

    Datatype

    boolean

    Alias
    UMLS CUI 2011AA
    C2242529
    MedDRA 14.1
    10067862
    UMLS CUI 2011AA
    C0884358
    SNOMED CT 2011_0131
    398166005
    UMLS CUI 2011AA
    C0008976
    SNOMED CT 2011_0131
    110465008
    UMLS CUI 2011AA
    C0679823
    HL7 V3 2006_05
    PART
    UMLS CUI 2011AA
    C0205099
    SNOMED CT 2011_0131
    26216008
    Ausschlusskriterien
    Beschrijving

    Ausschlusskriterien

    age at time of initial diagnosis or relapse diagnosis, respectively above 18 years
    Beschrijving

    age at time of initial diagnosis or relapse diagnosis, respectively above 18 years

    Datatype

    boolean

    Alias
    UMLS CUI 2011AA
    C0001779
    SNOMED CT 2011_0131
    397669002
    UMLS CUI 2011AA
    C0439547
    SNOMED CT 2011_0131
    272105005
    UMLS CUI 2011AA
    C0205265
    SNOMED CT 2011_0131
    884001
    UMLS CUI 2011AA
    C0277556
    SNOMED CT 2011_0131
    58184002
    UMLS CUI 2011AA
    C0011900
    SNOMED CT 2011_0131
    439401001
    LOINC Version 232
    MTHU008876
    no indication for allogeneic HSCT
    Beschrijving

    no indication for allogeneic HSCT

    Datatype

    boolean

    Alias
    UMLS CUI 2011AA
    C0521090
    SNOMED CT 2011_0131
    71653005
    UMLS CUI 2011AA
    C2242529
    MedDRA 14.1
    10067862
    no complete remission before SCT
    Beschrijving

    no complete remission before SCT

    Datatype

    boolean

    Alias
    UMLS CUI 2011AA
    C0332197
    SNOMED CT 2011_0131
    2667000
    UMLS CUI 2011AA
    C0677874
    SNOMED CT 2011_0131
    103338009
    UMLS CUI 2011AA
    C0332152
    SNOMED CT 2011_0131
    288556008
    UMLS CUI 2011AA
    C1504389
    MedDRA 14.1
    10063581
    no written consent of the parents (legal guardian) and, if necessary, the minor patient via Informed Consent Form
    Beschrijving

    no written consent of the parents (legal guardian) and, if necessary, the minor patient via Informed Consent Form

    Datatype

    boolean

    Alias
    UMLS CUI 2011AA
    C1705492
    UMLS CUI 2011AA
    C1576874
    HL7 V3 2006_05
    WRITTEN
    UMLS CUI 2011AA
    C0009797
    UMLS CUI 2011AA
    C0030551
    SNOMED CT 2011_0131
    40683002
    HL7 V3 2006_05
    PARNT
    UMLS CUI 2011AA
    C0023226
    SNOMED CT 2011_0131
    58626002
    LOINC Version 232
    MTHU020628
    UMLS CUI 2011AA
    C0026193
    SNOMED CT 2011_0131
    410599005
    UMLS CUI 2011AA
    C0030705
    SNOMED CT 2011_0131
    116154003
    Schwangerschaft
    Beschrijving

    pregnancy

    Datatype

    boolean

    Alias
    UMLS CUI 2011AA
    C0032961
    SNOMED CT 2011_0131
    289908002
    MedDRA 14.1
    10036556
    LOINC Version 232
    MTHU035048
    Secondary malignant neoplastic disease
    Beschrijving

    secondary malignancy

    Datatype

    boolean

    Alias
    UMLS CUI 2011AA
    C0027627
    SNOMED CT 2011_0131
    128462008
    previous HSCT
    Beschrijving

    previous HSCT

    Datatype

    boolean

    Alias
    UMLS CUI 2011AA
    C0205156
    SNOMED CT 2011_0131
    9130008
    UMLS CUI 2011AA
    C2242529
    MedDRA 14.1
    10067862
    HSCT is not performed in a study participating centre.
    Beschrijving

    HSCT is not performed in a study participating centre.

    Datatype

    boolean

    Alias
    UMLS CUI 2011AA
    C2242529
    MedDRA 14.1
    10067862
    UMLS CUI 2011AA
    C1518422
    UMLS CUI 2011AA
    C0884358
    SNOMED CT 2011_0131
    398166005
    UMLS CUI 2011AA
    C0008976
    SNOMED CT 2011_0131
    110465008
    UMLS CUI 2011AA
    C0679823
    HL7 V3 2006_05
    PART
    UMLS CUI 2011AA
    C0205099
    SNOMED CT 2011_0131
    26216008
    Terug naar het begin van de pagina

    Similar models

    Eligibility

    1 Formulieren
    1. StudyEvent: Eligibility
      1. Eligibility
    Name
    Type
    Description | Question | Decode (Coded Value)
    Datatype
    Alias
    Item Group
    Einschlusskriterien
    age 3 Months to 18 Years
    Item
    Alter 3 Monate bis 18 Jahre
    boolean
    C0001779 (UMLS CUI 2011AA)
    397669002 (SNOMED CT 2011_0131)
    Lymphoblastic Leukemia, Acute, Childhood
    Item
    Lymphoblastic Leukemia, Acute, Childhood
    boolean
    C0023452 (UMLS CUI 2011AA)
    C0011900 (UMLS CUI 2011AA)
    439401001 (SNOMED CT 2011_0131)
    MTHU008876 (LOINC Version 232)
    age at time of initial diagnosis or relapse diagnosis, respectively under or equal 18 years
    Item
    age at time of initial diagnosis or relapse diagnosis, respectively under or equal 18 years
    boolean
    C0205265 (UMLS CUI 2011AA)
    884001 (SNOMED CT 2011_0131)
    C0277556 (UMLS CUI 2011AA)
    58184002 (SNOMED CT 2011_0131)
    C0011900 (UMLS CUI 2011AA)
    439401001 (SNOMED CT 2011_0131)
    MTHU008876 (LOINC Version 232)
    indication for allogeneic HSCT
    Item
    indication for allogeneic HSCT
    boolean
    CL335836 (UMLS CUI 2011AA)
    C2242529 (UMLS CUI 2011AA)
    10067862 (MedDRA 14.1)
    complete remission before HSCT
    Item
    complete remission before HSCT
    boolean
    C0677874 (UMLS CUI 2011AA)
    103338009 (SNOMED CT 2011_0131)
    C0332152 (UMLS CUI 2011AA)
    288556008 (SNOMED CT 2011_0131)
    C2242529 (UMLS CUI 2011AA)
    10067862 (MedDRA 14.1)
    written consent of the parents (legal guardian) and, if necessary, the minor patient via Informed Consent Form
    Item
    written consent of the parents (legal guardian) and, if necessary, the minor patient via Informed Consent Form
    boolean
    C1576874 (UMLS CUI 2011AA)
    WRITTEN (HL7 V3 2006_05)
    C0009797 (UMLS CUI 2011AA)
    C0030551 (UMLS CUI 2011AA)
    40683002 (SNOMED CT 2011_0131)
    PARNT (HL7 V3 2006_05)
    C0023226 (UMLS CUI 2011AA)
    58626002 (SNOMED CT 2011_0131)
    MTHU020628 (LOINC Version 232)
    C0026193 (UMLS CUI 2011AA)
    410599005 (SNOMED CT 2011_0131)
    C0030705 (UMLS CUI 2011AA)
    116154003 (SNOMED CT 2011_0131)
    no pregnancy
    Item
    nicht schwanger
    boolean
    C0232973 (UMLS CUI 2011AA)
    60001007 (SNOMED CT 2011_0131)
    no secondary malignancy
    Item
    no secondary malignancy
    boolean
    C0332197 (UMLS CUI 2011AA)
    2667000 (SNOMED CT 2011_0131)
    C0027627 (UMLS CUI 2011AA)
    128462008 (SNOMED CT 2011_0131)
    no previous HSCT
    Item
    no previous HSCT
    boolean
    C0332197 (UMLS CUI 2011AA)
    2667000 (SNOMED CT 2011_0131)
    C0205156 (UMLS CUI 2011AA)
    9130008 (SNOMED CT 2011_0131)
    C2242529 (UMLS CUI 2011AA)
    10067862 (MedDRA 14.1)
    HSCT is performed in a study participating centre.
    Item
    HSCT is performed in a study participating centre.
    boolean
    C2242529 (UMLS CUI 2011AA)
    10067862 (MedDRA 14.1)
    C0884358 (UMLS CUI 2011AA)
    398166005 (SNOMED CT 2011_0131)
    C0008976 (UMLS CUI 2011AA)
    110465008 (SNOMED CT 2011_0131)
    C0679823 (UMLS CUI 2011AA)
    PART (HL7 V3 2006_05)
    C0205099 (UMLS CUI 2011AA)
    26216008 (SNOMED CT 2011_0131)
    Item Group
    Ausschlusskriterien
    age at time of initial diagnosis or relapse diagnosis, respectively above 18 years
    Item
    age at time of initial diagnosis or relapse diagnosis, respectively above 18 years
    boolean
    C0001779 (UMLS CUI 2011AA)
    397669002 (SNOMED CT 2011_0131)
    C0439547 (UMLS CUI 2011AA)
    272105005 (SNOMED CT 2011_0131)
    C0205265 (UMLS CUI 2011AA)
    884001 (SNOMED CT 2011_0131)
    C0277556 (UMLS CUI 2011AA)
    58184002 (SNOMED CT 2011_0131)
    C0011900 (UMLS CUI 2011AA)
    439401001 (SNOMED CT 2011_0131)
    MTHU008876 (LOINC Version 232)
    no indication for allogeneic HSCT
    Item
    no indication for allogeneic HSCT
    boolean
    C0521090 (UMLS CUI 2011AA)
    71653005 (SNOMED CT 2011_0131)
    C2242529 (UMLS CUI 2011AA)
    10067862 (MedDRA 14.1)
    no complete remission before SCT
    Item
    no complete remission before SCT
    boolean
    C0332197 (UMLS CUI 2011AA)
    2667000 (SNOMED CT 2011_0131)
    C0677874 (UMLS CUI 2011AA)
    103338009 (SNOMED CT 2011_0131)
    C0332152 (UMLS CUI 2011AA)
    288556008 (SNOMED CT 2011_0131)
    C1504389 (UMLS CUI 2011AA)
    10063581 (MedDRA 14.1)
    no written consent of the parents (legal guardian) and, if necessary, the minor patient via Informed Consent Form
    Item
    no written consent of the parents (legal guardian) and, if necessary, the minor patient via Informed Consent Form
    boolean
    C1705492 (UMLS CUI 2011AA)
    C1576874 (UMLS CUI 2011AA)
    WRITTEN (HL7 V3 2006_05)
    C0009797 (UMLS CUI 2011AA)
    C0030551 (UMLS CUI 2011AA)
    40683002 (SNOMED CT 2011_0131)
    PARNT (HL7 V3 2006_05)
    C0023226 (UMLS CUI 2011AA)
    58626002 (SNOMED CT 2011_0131)
    MTHU020628 (LOINC Version 232)
    C0026193 (UMLS CUI 2011AA)
    410599005 (SNOMED CT 2011_0131)
    C0030705 (UMLS CUI 2011AA)
    116154003 (SNOMED CT 2011_0131)
    pregnancy
    Item
    Schwangerschaft
    boolean
    C0032961 (UMLS CUI 2011AA)
    289908002 (SNOMED CT 2011_0131)
    10036556 (MedDRA 14.1)
    MTHU035048 (LOINC Version 232)
    secondary malignancy
    Item
    Secondary malignant neoplastic disease
    boolean
    C0027627 (UMLS CUI 2011AA)
    128462008 (SNOMED CT 2011_0131)
    previous HSCT
    Item
    previous HSCT
    boolean
    C0205156 (UMLS CUI 2011AA)
    9130008 (SNOMED CT 2011_0131)
    C2242529 (UMLS CUI 2011AA)
    10067862 (MedDRA 14.1)
    HSCT is not performed in a study participating centre.
    Item
    HSCT is not performed in a study participating centre.
    boolean
    C2242529 (UMLS CUI 2011AA)
    10067862 (MedDRA 14.1)
    C1518422 (UMLS CUI 2011AA)
    C0884358 (UMLS CUI 2011AA)
    398166005 (SNOMED CT 2011_0131)
    C0008976 (UMLS CUI 2011AA)
    110465008 (SNOMED CT 2011_0131)
    C0679823 (UMLS CUI 2011AA)
    PART (HL7 V3 2006_05)
    C0205099 (UMLS CUI 2011AA)
    26216008 (SNOMED CT 2011_0131)
    Terug naar het begin van de pagina 

    Help

    Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

    Watch Tutorial