0 Beoordelingen
ID

13727

Beschrijving

Intensity Modulated Total Marrow Irradiation (IM-TMI) for Advanced Hematologic Malignancies; ODM derived from: https://clinicaltrials.gov/show/NCT00988013

Link

https://clinicaltrials.gov/show/NCT00988013

Trefwoorden

Versies (1)
  1. 01-03-16 01-03-16 -
Houder van rechten

CC BY-NC 3.0

Geüploaded op

1 maart 2016

DOI

Voor een aanvraag inloggen.

Licentie

Creative Commons BY-NC 3.0
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 Acute Myeloid Leukemia NCT00988013

    Engels

    Eligibility Acute Myeloid Leukemia NCT00988013

    1 Formulieren  
    Inclusion Criteria
    Beschrijving

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693 (Inclusion)
    patients with the following diseases: acute myeloid or lymphoblastic leukemia in first complete remission if poor prognosis documented by failure to response after initial induction chemotherapy, or cytogenetic, or molecular studies. acute leukemia in greater/equal second remission, or partial remission after chemotherapy. high grade non hodgkin's or hodgkin's lymphoma with marrow involvement resistant/ relapsed after second line therapy including high dose chemotherapy and autologous sct. cml in advanced or blastic phase. plasma cell leukemia.
    Beschrijving

    patients with the following diseases: acute myeloid or lymphoblastic leukemia in first complete remission if poor prognosis documented by failure to response after initial induction chemotherapy, or cytogenetic, or molecular studies. acute leukemia in greater/equal second remission, or partial remission after chemotherapy. high grade non hodgkin's or hodgkin's lymphoma with marrow involvement resistant/ relapsed after second line therapy including high dose chemotherapy and autologous sct. cml in advanced or blastic phase. plasma cell leukemia.

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0023467 (Leukemia, Myelocytic, Acute)
    SNOMED
    17788007
    UMLS CUI [2]
    C0023474 (Leukemia, Myeloid, Chronic-Phase)
    SNOMED
    413847001
    UMLS CUI [3]
    C0023449 (Acute lymphocytic leukemia)
    SNOMED
    91857003
    LOINC
    LA31346-2
    UMLS CUI [4]
    C0019829 (Hodgkin Disease)
    SNOMED
    14537002
    UMLS CUI [5]
    C0024305 (Lymphoma, Non-Hodgkin)
    SNOMED
    1929004
    UMLS CUI [6]
    C0023484 (Leukemia, Plasma Cell)
    SNOMED
    95210003
    age 18-60 years.
    Beschrijving

    age 18-60 years.

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0001779 (Age)
    SNOMED
    424144002
    LOINC
    LP28815-6
    karnofsky performance status of 70
    Beschrijving

    karnofsky performance status of 70

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0206065 (Karnofsky Performance Status)
    SNOMED
    273546003
    LOINC
    LP267177-6
    adequate cardiac and pulmonary function. patients with decreased lvef less than/equal to 40% or dlco less than/equal to 50% of predicted will require clearance from cardiology or pulmonary services, respectively, prior to enrollment on this protocol.
    Beschrijving

    adequate cardiac and pulmonary function. patients with decreased lvef less than/equal to 40% or dlco less than/equal to 50% of predicted will require clearance from cardiology or pulmonary services, respectively, prior to enrollment on this protocol.

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0428772 (Left ventricular ejection fraction)
    SNOMED
    250908004
    UMLS CUI [2]
    C1516251 (Carbon Monoxide Diffusing Capability Test)
    serum creatinine less than/equal to 1.5 mg/dl or creatinine clearance greater than/equal to 50 ml/min .
    Beschrijving

    serum creatinine less than/equal to 1.5 mg/dl or creatinine clearance greater than/equal to 50 ml/min .

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0201976 (Creatinine measurement, serum (procedure))
    SNOMED
    113075003
    UMLS CUI [2]
    C0373595 (Creatinine clearance measurement)
    SNOMED
    167181009
    serum bilirubin 2.0 mg/dl, sgpt less than/equal to 3 times the upper limit of normal
    Beschrijving

    serum bilirubin 2.0 mg/dl, sgpt less than/equal to 3 times the upper limit of normal

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C1278039 (Serum total bilirubin measurement)
    SNOMED
    313840000
    UMLS CUI [2]
    C0201836 (Alanine aminotransferase measurement)
    SNOMED
    34608000
    Exclusion Criteria
    Beschrijving

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251 (Exclusion Criteria)
    life expectancy is severely limited by concomitant illness.
    Beschrijving

    life expectancy is severely limited by concomitant illness.

    Datatype

    boolean

    Alias
    UMLS CUI [1,1]
    C0023671 (Life Expectancy)
    UMLS CUI [1,2]
    C0439801 (Limited (extensiveness))
    SNOMED
    255469002
    LOINC
    LP34047-8
    UMLS CUI [1,3]
    C0009488 (Comorbidity)
    evidence of chronic active hepatitis or cirrhosis
    Beschrijving

    evidence of chronic active hepatitis or cirrhosis

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0019158 (Hepatitis)
    SNOMED
    128241005
    LOINC
    LP20771-9
    UMLS CUI [2]
    C0023890 (Liver Cirrhosis)
    SNOMED
    19943007
    hiv-positive
    Beschrijving

    hiv-positive

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0019682 (HIV)
    SNOMED
    19030005
    LOINC
    LP17126-1
    patient is pregnant
    Beschrijving

    patient is pregnant

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0032961 (Pregnancy)
    SNOMED
    289908002
    LOINC
    LP75920-6
    patient or guardian is not able to sign informed consent.
    Beschrijving

    patient or guardian is not able to sign informed consent.

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0021430 (Informed Consent)
    Terug naar het begin van de pagina

    Similar models

    Eligibility Acute Myeloid Leukemia NCT00988013

    1 Formulieren
    Name
    Type
    Description | Question | Decode (Coded Value)
    Datatype
    Alias
    Item Group
    C1512693 (UMLS CUI)
    patients with the following diseases:
    Item
    patients with the following diseases: acute myeloid or lymphoblastic leukemia in first complete remission if poor prognosis documented by failure to response after initial induction chemotherapy, or cytogenetic, or molecular studies. acute leukemia in greater/equal second remission, or partial remission after chemotherapy. high grade non hodgkin's or hodgkin's lymphoma with marrow involvement resistant/ relapsed after second line therapy including high dose chemotherapy and autologous sct. cml in advanced or blastic phase. plasma cell leukemia.
    boolean
    C0023467 (UMLS CUI [1])
    C0023474 (UMLS CUI [2])
    C0023449 (UMLS CUI [3])
    C0019829 (UMLS CUI [4])
    C0024305 (UMLS CUI [5])
    C0023484 (UMLS CUI [6])
    age
    Item
    age 18-60 years.
    boolean
    C0001779 (UMLS CUI [1])
    karnofsky
    Item
    karnofsky performance status of 70
    boolean
    C0206065 (UMLS CUI [1])
    cardiac and pulmonary function
    Item
    adequate cardiac and pulmonary function. patients with decreased lvef less than/equal to 40% or dlco less than/equal to 50% of predicted will require clearance from cardiology or pulmonary services, respectively, prior to enrollment on this protocol.
    boolean
    C0428772 (UMLS CUI [1])
    C1516251 (UMLS CUI [2])
    creatinine or creatinine clearance
    Item
    serum creatinine less than/equal to 1.5 mg/dl or creatinine clearance greater than/equal to 50 ml/min .
    boolean
    C0201976 (UMLS CUI [1])
    C0373595 (UMLS CUI [2])
    bilirubin
    Item
    serum bilirubin 2.0 mg/dl, sgpt less than/equal to 3 times the upper limit of normal
    boolean
    C1278039 (UMLS CUI [1])
    C0201836 (UMLS CUI [2])
    Item Group
    C0680251 (UMLS CUI)
    life expectancy is severely limited by concomitant illness.
    Item
    life expectancy is severely limited by concomitant illness.
    boolean
    C0023671 (UMLS CUI [1,1])
    C0439801 (UMLS CUI [1,2])
    C0009488 (UMLS CUI [1,3])
    hepatitis
    Item
    evidence of chronic active hepatitis or cirrhosis
    boolean
    C0019158 (UMLS CUI [1])
    C0023890 (UMLS CUI [2])
    hiv
    Item
    hiv-positive
    boolean
    C0019682 (UMLS CUI [1])
    pregnancy
    Item
    patient is pregnant
    boolean
    C0032961 (UMLS CUI [1])
    patient or guardian is not able to sign informed consent.
    Item
    patient or guardian is not able to sign informed consent.
    boolean
    C0021430 (UMLS CUI [1])
    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