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ID

24517

Description

A Phase I Trial of Alloreactive Cell Infusion Following Transplantation of Haplotype Cells in Patients With Myeloid Malignancies; ODM derived from: https://clinicaltrials.gov/show/NCT00569179

Lien

https://clinicaltrials.gov/show/NCT00569179

Mots-clés

  1. 04/08/2017 04/08/2017 -
Téléchargé le

4 août 2017

DOI

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Licence

Creative Commons BY 4.0

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    Eligibility Leukemia, Myeloid, Acute NCT00569179

    Eligibility Leukemia, Myeloid, Acute NCT00569179

    Inclusion Criteria
    Description

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693
    patients must have histologically documented aml, all, mds, cml,
    Description

    Leukemia, Myelocytic, Acute | Acute lymphocytic leukemia | MYELODYSPLASTIC SYNDROME | Myeloid Leukemia, Chronic

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0023467
    UMLS CUI [2]
    C0023449
    UMLS CUI [3]
    C3463824
    UMLS CUI [4]
    C0023473
    identification of haploidentical donor
    Description

    Haploidentical donor Identification

    Type de données

    boolean

    Alias
    UMLS CUI [1,1]
    C3829897
    UMLS CUI [1,2]
    C0205396
    lvef > 45% corrected
    Description

    Left ventricular ejection fraction

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0428772
    dlco > 50% predicted
    Description

    Carbon Monoxide Diffusing Capability Test

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C1516251
    serum creatinine <= 2 mg/dl
    Description

    Creatinine measurement, serum

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0201976
    bilirubin < 2 x uln
    Description

    Serum total bilirubin measurement

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C1278039
    ast, alt < 2 x uln
    Description

    Aspartate aminotransferase measurement | Alanine aminotransferase measurement

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0201899
    UMLS CUI [2]
    C0201836
    age ≤ 65 years
    Description

    Age

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0001779
    performance status 0-1
    Description

    performance status

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C1518965
    Exclusion Criteria
    Description

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251
    patients relapsing <6 months after autologous sct are not eligible.
    Description

    Recurrent disease Post Transplantation of autologous hematopoietic stem cell

    Type de données

    boolean

    Alias
    UMLS CUI [1,1]
    C0277556
    UMLS CUI [1,2]
    C0687676
    UMLS CUI [1,3]
    C1831743
    patients with active infections requiring oral or intravenous antibiotics are not eligible for enrollment until resolution of infection
    Description

    Communicable Diseases Requirement Oral antibiotic therapy | Communicable Diseases Requirement Intravenous antibiotic therapy

    Type de données

    boolean

    Alias
    UMLS CUI [1,1]
    C0009450
    UMLS CUI [1,2]
    C1514873
    UMLS CUI [1,3]
    C0559681
    UMLS CUI [2,1]
    C0009450
    UMLS CUI [2,2]
    C1514873
    UMLS CUI [2,3]
    C0559680
    no hiv disease
    Description

    HIV Infection

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0019693
    non-pregnant and non-nursing
    Description

    Pregnancy | Breast Feeding

    Type de données

    boolean

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

    Similar models

    Eligibility Leukemia, Myeloid, Acute NCT00569179

    Name
    Type
    Description | Question | Decode (Coded Value)
    Type de données
    Alias
    Item Group
    C1512693 (UMLS CUI)
    Leukemia, Myelocytic, Acute | Acute lymphocytic leukemia | MYELODYSPLASTIC SYNDROME | Myeloid Leukemia, Chronic
    Item
    patients must have histologically documented aml, all, mds, cml,
    boolean
    C0023467 (UMLS CUI [1])
    C0023449 (UMLS CUI [2])
    C3463824 (UMLS CUI [3])
    C0023473 (UMLS CUI [4])
    Haploidentical donor Identification
    Item
    identification of haploidentical donor
    boolean
    C3829897 (UMLS CUI [1,1])
    C0205396 (UMLS CUI [1,2])
    Left ventricular ejection fraction
    Item
    lvef > 45% corrected
    boolean
    C0428772 (UMLS CUI [1])
    Carbon Monoxide Diffusing Capability Test
    Item
    dlco > 50% predicted
    boolean
    C1516251 (UMLS CUI [1])
    Creatinine measurement, serum
    Item
    serum creatinine <= 2 mg/dl
    boolean
    C0201976 (UMLS CUI [1])
    Serum total bilirubin measurement
    Item
    bilirubin < 2 x uln
    boolean
    C1278039 (UMLS CUI [1])
    Aspartate aminotransferase measurement | Alanine aminotransferase measurement
    Item
    ast, alt < 2 x uln
    boolean
    C0201899 (UMLS CUI [1])
    C0201836 (UMLS CUI [2])
    Age
    Item
    age ≤ 65 years
    boolean
    C0001779 (UMLS CUI [1])
    performance status
    Item
    performance status 0-1
    boolean
    C1518965 (UMLS CUI [1])
    Item Group
    C0680251 (UMLS CUI)
    Recurrent disease Post Transplantation of autologous hematopoietic stem cell
    Item
    patients relapsing <6 months after autologous sct are not eligible.
    boolean
    C0277556 (UMLS CUI [1,1])
    C0687676 (UMLS CUI [1,2])
    C1831743 (UMLS CUI [1,3])
    Communicable Diseases Requirement Oral antibiotic therapy | Communicable Diseases Requirement Intravenous antibiotic therapy
    Item
    patients with active infections requiring oral or intravenous antibiotics are not eligible for enrollment until resolution of infection
    boolean
    C0009450 (UMLS CUI [1,1])
    C1514873 (UMLS CUI [1,2])
    C0559681 (UMLS CUI [1,3])
    C0009450 (UMLS CUI [2,1])
    C1514873 (UMLS CUI [2,2])
    C0559680 (UMLS CUI [2,3])
    HIV Infection
    Item
    no hiv disease
    boolean
    C0019693 (UMLS CUI [1])
    Pregnancy | Breast Feeding
    Item
    non-pregnant and non-nursing
    boolean
    C0032961 (UMLS CUI [1])
    C0006147 (UMLS CUI [2])

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