ID

15296

Beschreibung

Study of Rituximab Plus High-Dose Chemotherapy Non-Hodgkin's Lymphoma; ODM derived from: https://clinicaltrials.gov/show/NCT00143871

Link

https://clinicaltrials.gov/show/NCT00143871

Stichworte

  1. 25.05.16 25.05.16 -
Hochgeladen am

25. Mai 2016

DOI

Für eine Beantragung loggen Sie sich ein.

Lizenz

Creative Commons BY 4.0

Modell Kommentare :

Hier können Sie das Modell kommentieren. Über die Sprechblasen an den Itemgruppen und Items können Sie diese spezifisch kommentieren.

Itemgroup Kommentare für :

Item Kommentare für :


    Keine Kommentare

    Um Formulare herunterzuladen müssen Sie angemeldet sein. Bitte loggen Sie sich ein oder registrieren Sie sich kostenlos.

    Eligibility Lymphoma, Non-Hodgkin's NCT00143871

    Eligibility Lymphoma, Non-Hodgkin's NCT00143871

    Inclusion Criteria
    Beschreibung

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693
    histologically documented, aggressive and/ or intermediate grade and high-grade b cell nhl, cd20 positive.
    Beschreibung

    b-cell NHL

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C1512431
    UMLS CUI [2]
    C1512858
    in relapse after primary conventional chemotherapy
    Beschreibung

    chemotherapy

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0392920
    tumor sensitive (at least a partial response) to induction chemotherapy and/ or radiation therapy after treatment for relapse
    Beschreibung

    tumor sensitive

    Datentyp

    boolean

    Alias
    UMLS CUI [1,1]
    C1704632
    UMLS CUI [1,2]
    C0392920
    UMLS CUI [2,1]
    C1704632
    UMLS CUI [2,2]
    C1522449
    treatment of cns or meningeal disease (cytology-negative csf) if present
    Beschreibung

    treatment of cns or meningeal disease

    Datentyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0087111
    UMLS CUI [1,2]
    C0007682
    UMLS CUI [2,1]
    C0087111
    UMLS CUI [2,2]
    C0154728
    cumulative total doxorubicin dosage <500 mg/m2
    Beschreibung

    doxorubicin dosage

    Datentyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0013089
    UMLS CUI [1,2]
    C0178602
    performance score: 0-2
    Beschreibung

    performance score

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C1518965
    prior malignancies eligible if treated for cure and without active disease
    Beschreibung

    prior malignancies

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0006826
    patients must not be pregnant or nursing.
    Beschreibung

    pregnant or nursing

    Datentyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0032961
    UMLS CUI [1,2]
    C0006147
    prior immunotherapy is allowed
    Beschreibung

    prior immunotherapy

    Datentyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0021083
    UMLS CUI [1,2]
    C0332152
    signed informed consent
    Beschreibung

    signed informed consent

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0021430
    absolute neutrophil count > 1500/ µl, platelet count >100,000/ µl
    Beschreibung

    neutrophil count and platelet count

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0200633
    UMLS CUI [2]
    C0005821
    bilirubin <1.5 x normal, sgot <2.5 x normal
    Beschreibung

    bilirubin and sgot

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0005437
    UMLS CUI [2]
    C0201899
    serum creatinine <1.5 mg/dl
    Beschreibung

    serum creatinine

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0201976
    ejection fraction > 45% or > 40% with normal wall motion
    Beschreibung

    ejection fraction

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0232174
    hiv negative
    Beschreibung

    hiv negative

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0481430
    fev1, dlco > 50% predicted
    Beschreibung

    fev1

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0748133
    Exclusion Criteria
    Beschreibung

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251
    pregnant or nursing
    Beschreibung

    pregnant or nursing

    Datentyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0032961
    UMLS CUI [1,2]
    C0006147

    Ähnliche Modelle

    Eligibility Lymphoma, Non-Hodgkin's NCT00143871

    Name
    Typ
    Description | Question | Decode (Coded Value)
    Datentyp
    Alias
    Item Group
    C1512693 (UMLS CUI)
    b-cell NHL
    Item
    histologically documented, aggressive and/ or intermediate grade and high-grade b cell nhl, cd20 positive.
    boolean
    C1512431 (UMLS CUI [1])
    C1512858 (UMLS CUI [2])
    chemotherapy
    Item
    in relapse after primary conventional chemotherapy
    boolean
    C0392920 (UMLS CUI [1])
    tumor sensitive
    Item
    tumor sensitive (at least a partial response) to induction chemotherapy and/ or radiation therapy after treatment for relapse
    boolean
    C1704632 (UMLS CUI [1,1])
    C0392920 (UMLS CUI [1,2])
    C1704632 (UMLS CUI [2,1])
    C1522449 (UMLS CUI [2,2])
    treatment of cns or meningeal disease
    Item
    treatment of cns or meningeal disease (cytology-negative csf) if present
    boolean
    C0087111 (UMLS CUI [1,1])
    C0007682 (UMLS CUI [1,2])
    C0087111 (UMLS CUI [2,1])
    C0154728 (UMLS CUI [2,2])
    doxorubicin dosage
    Item
    cumulative total doxorubicin dosage <500 mg/m2
    boolean
    C0013089 (UMLS CUI [1,1])
    C0178602 (UMLS CUI [1,2])
    performance score
    Item
    performance score: 0-2
    boolean
    C1518965 (UMLS CUI [1])
    prior malignancies
    Item
    prior malignancies eligible if treated for cure and without active disease
    boolean
    C0006826 (UMLS CUI [1])
    pregnant or nursing
    Item
    patients must not be pregnant or nursing.
    boolean
    C0032961 (UMLS CUI [1,1])
    C0006147 (UMLS CUI [1,2])
    prior immunotherapy
    Item
    prior immunotherapy is allowed
    boolean
    C0021083 (UMLS CUI [1,1])
    C0332152 (UMLS CUI [1,2])
    signed informed consent
    Item
    signed informed consent
    boolean
    C0021430 (UMLS CUI [1])
    neutrophil count and platelet count
    Item
    absolute neutrophil count > 1500/ µl, platelet count >100,000/ µl
    boolean
    C0200633 (UMLS CUI [1])
    C0005821 (UMLS CUI [2])
    bilirubin and sgot
    Item
    bilirubin <1.5 x normal, sgot <2.5 x normal
    boolean
    C0005437 (UMLS CUI [1])
    C0201899 (UMLS CUI [2])
    serum creatinine
    Item
    serum creatinine <1.5 mg/dl
    boolean
    C0201976 (UMLS CUI [1])
    ejection fraction
    Item
    ejection fraction > 45% or > 40% with normal wall motion
    boolean
    C0232174 (UMLS CUI [1])
    hiv negative
    Item
    hiv negative
    boolean
    C0481430 (UMLS CUI [1])
    fev1
    Item
    fev1, dlco > 50% predicted
    boolean
    C0748133 (UMLS CUI [1])
    Item Group
    C0680251 (UMLS CUI)
    pregnant or nursing
    Item
    pregnant or nursing
    boolean
    C0032961 (UMLS CUI [1,1])
    C0006147 (UMLS CUI [1,2])

    Benötigen Sie Hilfe bei der Suche? Um mehr Details zu erfahren und die Suche effektiver nutzen zu können schauen Sie sich doch das entsprechende Video auf unserer Tutorial Seite an.

    Zum Video