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ID

32551

Beschreibung

A Phase II Study of Single-Agent Lenalidomide in Subjects With Relapsed Or Refractory T-Cell Non-Hodgkin's Lymphoma; ODM derived from: https://clinicaltrials.gov/show/NCT00655668

Link

https://clinicaltrials.gov/show/NCT00655668

Stichworte

  1. 06.11.18 06.11.18 -
Rechteinhaber

See clinicaltrials.gov

Hochgeladen am

6. November 2018

DOI

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Lizenz

Creative Commons BY 4.0

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    Eligibility T-cell Non-Hodgkin's Lymphoma NCT00655668

    Eligibility T-cell Non-Hodgkin's Lymphoma NCT00655668

    Inclusion Criteria
    Beschreibung

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693
    must understand and voluntarily sign an informed consent form.
    Beschreibung

    Informed Consent

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0021430
    must be ≥ 18 years of age at the time of signing the informed consent form.
    Beschreibung

    Age

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0001779
    must be able to adhere to the study visit schedule and other protocol requirements.
    Beschreibung

    Protocol Compliance

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0525058
    biopsy-proven t-cell non-hodgkin's lymphoma, either:
    Beschreibung

    T-Cell Lymphoma

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0079772
    peripheral t-cell lymphoma (ptcl) whatever the subtype, or
    Beschreibung

    Peripheral T-Cell Lymphoma Subtype Any

    Datentyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0079774
    UMLS CUI [1,2]
    C0449560
    UMLS CUI [1,3]
    C1552551
    cutaneous t-cell lymphoma (ctcl), but only the subtype mycosis fungoides.
    Beschreibung

    Cutaneous t-cell lymphoma/Mycosis fungoides

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0026948
    relapsed or refractory to previous therapy for t-cell non-hodgkin's lymphoma.
    Beschreibung

    Prior Therapy | T-cell lymphoma recurrent | T-cell lymphoma refractory

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C1514463
    UMLS CUI [2]
    C0854826
    UMLS CUI [3]
    C0854827
    must have received at least one prior combination chemotherapy regimen. there is no limit on the number of prior therapies.
    Beschreibung

    Combination Chemotherapy Quantity

    Datentyp

    boolean

    Alias
    UMLS CUI [1,1]
    C1521750
    UMLS CUI [1,2]
    C1265611
    Exclusion Criteria
    Beschreibung

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251
    cutaneous t-cell lymphoma of subtype sézary syndrome.
    Beschreibung

    Cutaneous T-cell lymphoma/Sezary Syndrome

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0036920

    Ähnliche Modelle

    Eligibility T-cell Non-Hodgkin's Lymphoma NCT00655668

    Name
    Typ
    Description | Question | Decode (Coded Value)
    Datentyp
    Alias
    Item Group
    C1512693 (UMLS CUI)
    Informed Consent
    Item
    must understand and voluntarily sign an informed consent form.
    boolean
    C0021430 (UMLS CUI [1])
    Age
    Item
    must be ≥ 18 years of age at the time of signing the informed consent form.
    boolean
    C0001779 (UMLS CUI [1])
    Protocol Compliance
    Item
    must be able to adhere to the study visit schedule and other protocol requirements.
    boolean
    C0525058 (UMLS CUI [1])
    T-Cell Lymphoma
    Item
    biopsy-proven t-cell non-hodgkin's lymphoma, either:
    boolean
    C0079772 (UMLS CUI [1])
    Peripheral T-Cell Lymphoma Subtype Any
    Item
    peripheral t-cell lymphoma (ptcl) whatever the subtype, or
    boolean
    C0079774 (UMLS CUI [1,1])
    C0449560 (UMLS CUI [1,2])
    C1552551 (UMLS CUI [1,3])
    Cutaneous t-cell lymphoma/Mycosis fungoides
    Item
    cutaneous t-cell lymphoma (ctcl), but only the subtype mycosis fungoides.
    boolean
    C0026948 (UMLS CUI [1])
    Prior Therapy | T-cell lymphoma recurrent | T-cell lymphoma refractory
    Item
    relapsed or refractory to previous therapy for t-cell non-hodgkin's lymphoma.
    boolean
    C1514463 (UMLS CUI [1])
    C0854826 (UMLS CUI [2])
    C0854827 (UMLS CUI [3])
    Combination Chemotherapy Quantity
    Item
    must have received at least one prior combination chemotherapy regimen. there is no limit on the number of prior therapies.
    boolean
    C1521750 (UMLS CUI [1,1])
    C1265611 (UMLS CUI [1,2])
    Item Group
    C0680251 (UMLS CUI)
    Cutaneous T-cell lymphoma/Sezary Syndrome
    Item
    cutaneous t-cell lymphoma of subtype sézary syndrome.
    boolean
    C0036920 (UMLS CUI [1])

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