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ID

13021

Description

Cyclophosphamide and Total Body Irradiation in Treating Patients Who Are Undergoing an Autologous Peripheral Stem Cell Transplant For Chronic Lymphocytic Leukemia; ODM derived from: https://clinicaltrials.gov/show/NCT00275015

Link

https://clinicaltrials.gov/show/NCT00275015

Keywords

  1. 1/12/16 1/12/16 -
Copyright Holder

CC BY-NC 3.0

Uploaded on

January 12, 2016

DOI

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License

Creative Commons BY-NC 3.0

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    Eligibility Leukemia NCT00275015

    Eligibility Leukemia NCT00275015

    1. StudyEvent: Eligibility
      1. Eligibility Leukemia NCT00275015
    Criteria
    Description

    Criteria

    patients with chronic lymphocytic leukemia, meeting 1 of the following criteria:
    Description

    CLL

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0023434 (Chronic Lymphocytic Leukemia)
    SNOMED
    51092000
    LOINC
    LP34550-1
    binet stage b or c disease
    Description

    binet stage

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C1511118 (Binet Staging System)
    binet stage a disease and at high risk for disease progression, defined as the following:
    Description

    binet stage a disease and at high risk for disease progression

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C1511118 (Binet Staging System)
    non-nodular marrow infiltration or lymphocyte doubling time < 12 months
    Description

    non-nodular marrow infiltration or lymphocyte doubling time < 12 months

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C3854434 (Bone marrow infiltration)
    UMLS CUI [2]
    C2986483 (Doubling Time)
    thymidine kinase > 7.0 u/l or ß-2-microglobulin > 3.5 mg/l
    Description

    thymidine kinase, ß-2-microglobulin

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0040078 (Thymidine Kinase)
    SNOMED
    61588000
    UMLS CUI [2]
    C0005149 (beta-2 Microglobulin)
    SNOMED
    90945000
    polymerase chain reaction-amplifiable clonal cdriii rearrangement of the igv_h
    Description

    polymerase chain reaction-amplifiable clonal cdriii rearrangement of the igv_h

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0887928 (Complementarity Determining Region 3)
    ecog performance status 0-1
    Description

    ecog performance status

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C1520224 (ECOG performance status)
    SNOMED
    423740007
    no concurrent disease resulting in major organ dysfunction
    Description

    no concurrent disease resulting in major organ dysfunction

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0009488 (Comorbidity)
    no prior combination therapy comprising melphalan, dexamethasone, carmustine, cytarabine, and etoposide (dexa-beam)
    Description

    no prior combination therapy comprising melphalan, dexamethasone, carmustine, cytarabine, and etoposide (dexa-beam)

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0025241 (melphalan)
    SNOMED
    544002
    UMLS CUI [2]
    C0011777 (dexamethasone)
    SNOMED
    7561000
    UMLS CUI [3]
    C0007257 (carmustine)
    SNOMED
    51326002
    UMLS CUI [4]
    C0010711 (cytarabine)
    SNOMED
    89265009
    UMLS CUI [5]
    C0015133 (etoposide)
    SNOMED
    56928005
    no more than 1 prior chemotherapy regimen
    Description

    no more than 1 prior chemotherapy regimen

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0392920 (Chemotherapy Regimen)
    SNOMED
    716872004
    no prior chemotherapy regimen longer than 6 months in duration
    Description

    no prior chemotherapy regimen longer than 6 months in duration

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0392920 (Chemotherapy Regimen)
    SNOMED
    716872004

    Similar models

    Eligibility Leukemia NCT00275015

    1. StudyEvent: Eligibility
      1. Eligibility Leukemia NCT00275015
    Name
    Type
    Description | Question | Decode (Coded Value)
    Data type
    Alias
    Item Group
    CLL
    Item
    patients with chronic lymphocytic leukemia, meeting 1 of the following criteria:
    boolean
    C0023434 (UMLS CUI [1])
    binet stage
    Item
    binet stage b or c disease
    boolean
    C1511118 (UMLS CUI [1])
    binet stage a disease and at high risk for disease progression
    Item
    binet stage a disease and at high risk for disease progression, defined as the following:
    boolean
    C1511118 (UMLS CUI [1])
    non-nodular marrow infiltration or lymphocyte doubling time < 12 months
    Item
    non-nodular marrow infiltration or lymphocyte doubling time < 12 months
    boolean
    C3854434 (UMLS CUI [1])
    C2986483 (UMLS CUI [2])
    thymidine kinase, ß-2-microglobulin
    Item
    thymidine kinase > 7.0 u/l or ß-2-microglobulin > 3.5 mg/l
    boolean
    C0040078 (UMLS CUI [1])
    C0005149 (UMLS CUI [2])
    polymerase chain reaction-amplifiable clonal cdriii rearrangement of the igv_h
    Item
    polymerase chain reaction-amplifiable clonal cdriii rearrangement of the igv_h
    boolean
    C0887928 (UMLS CUI [1])
    ecog performance status
    Item
    ecog performance status 0-1
    boolean
    C1520224 (UMLS CUI [1])
    no concurrent disease resulting in major organ dysfunction
    Item
    no concurrent disease resulting in major organ dysfunction
    boolean
    C0009488 (UMLS CUI [1])
    no prior combination therapy comprising melphalan, dexamethasone, carmustine, cytarabine, and etoposide (dexa-beam)
    Item
    no prior combination therapy comprising melphalan, dexamethasone, carmustine, cytarabine, and etoposide (dexa-beam)
    boolean
    C0025241 (UMLS CUI [1])
    C0011777 (UMLS CUI [2])
    C0007257 (UMLS CUI [3])
    C0010711 (UMLS CUI [4])
    C0015133 (UMLS CUI [5])
    no more than 1 prior chemotherapy regimen
    Item
    no more than 1 prior chemotherapy regimen
    boolean
    C0392920 (UMLS CUI [1])
    no prior chemotherapy regimen longer than 6 months in duration
    Item
    no prior chemotherapy regimen longer than 6 months in duration
    boolean
    C0392920 (UMLS CUI [1])

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