0 Beoordelingen
ID

12119

Beschrijving

The Role of Induction Gemcitabine and Cisplatin in Locoregionally Advanced Nasopharyngeal Carcinoma in the Era of IMRT; ODM derived from: https://clinicaltrials.gov/show/NCT02460887

Link

https://clinicaltrials.gov/show/NCT02460887

Trefwoorden

Versies (1)
  1. 24-09-15 24-09-15 - Julian Varghese
Geüploaded op

24 september 2015

DOI

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Licentie

Creative Commons BY 4.0
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    Eligibility Nasopharyngeal Carcinoma NCT02460887

    Engels

    Eligibility Nasopharyngeal Carcinoma NCT02460887

    1 Formulieren  
    Inclusion Criteria
    Beschrijving

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693
    patients with newly histologically confirmed non-keratinizing nasopharyngeal carcinoma (including who ii or iii).
    Beschrijving

    Nasopharyngeal Nonkeratinizing Carcinoma

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C1334926
    tumor staged as t1-4n2-3或t3-4n0-1m0 (according to the 7th ajcc edition).
    Beschrijving

    AJCC tumor staging

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0441915
    satisfactory performance status: karnofsky scale (kps) ≥ 70.
    Beschrijving

    satisfactory performance status: karnofsky scale

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C1520224
    adequate marrow: leucocyte count ≥ 4000/μl, hemoglobin ≥ 90g/l and platelet count ≥
    Beschrijving

    platelet count; hemoglobin

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0023508
    UMLS CUI [2]
    C0005821
    UMLS CUI [3]
    C0019046
    adequate liver function: alanine aminotransferase (alt), aspartate aminotransferase (ast) < 1.5×upper limit of normal (uln) concomitant with alkaline phosphatase (alp) ≤ 2.5×uln
    Beschrijving

    alkaline phosphatase; concomitant; normal; liver; upper; ast; uln

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0376147
    UMLS CUI [2]
    C0242192
    UMLS CUI [3]
    C0201850
    and bilirubin ≤1.5×uln.
    Beschrijving

    bilirubin; uln

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C1278039
    adequate renal function: creatinine clearance ≥ 60 ml/min.
    Beschrijving

    creatinine clearance; renal function

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0373595
    patients must be informed of the investigational nature of this study and give written informed consent.
    Beschrijving

    written informed consent.; study

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0021430
    Exclusion Criteria
    Beschrijving

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251
    who type keratinizing squamous cell carcinoma or basaloid squamous cell carcinoma.
    Beschrijving

    Basaloid squamous cell carcinoma | Squamous cell carcinoma, keratinizing

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C1266005
    UMLS CUI [2]
    C0334247
    treatment with palliative intent.
    Beschrijving

    palliative; treatment; intent

    Datatype

    boolean

    Alias
    UMLS CUI [1,1]
    C0087111
    UMLS CUI [1,2]
    C1285530
    prior malignancy except adequately treated basal cell or squamous cell skin cancer, in situ cervical cancer.
    Beschrijving

    prior malignancy; cervical; squamous; cancer; skin

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0006826
    pregnancy or lactation (consider pregnancy test in women of child-bearing age and emphasize effective contraception during the treatment period).
    Beschrijving

    Patient currently pregnant | Lactating (finding)

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0549206
    UMLS CUI [2]
    C2828358
    history of previous rt (except for non-melanomatous skin cancers outside intended rt treatment volume).
    Beschrijving

    history of previous rt

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C1522449
    prior chemotherapy or surgery (except diagnostic) to primary tumor or nodes.
    Beschrijving

    prior chemotherapy; primary tumor; surgery; nodes

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0392920
    UMLS CUI [2,1]
    C0038894
    UMLS CUI [2,2]
    C0006826
    any severe intercurrent disease, which may bring unacceptable risk or affect the compliance of the trial, for example, unstable cardiac disease requiring treatment, renal disease, chronic hepatitis, diabetes with poor control (fasting plasma glucose > 1.5×uln), and emotional disturbance.
    Beschrijving

    Disease condition determination, uncontrolled | Compliance behavior | Heart Diseases; Unstable status | Kidney Diseases | Hepatitis, Chronic | Diabetes mellitus poor control | Emotional Disturbances

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0184774
    UMLS CUI [2]
    C1321605
    UMLS CUI [3,1]
    C0018799
    UMLS CUI [3,2]
    C0443343
    UMLS CUI [4]
    C0022658
    UMLS CUI [5]
    C0019189
    UMLS CUI [6]
    C0860161
    UMLS CUI [7]
    C0013985
    Terug naar het begin van de pagina

    Similar models

    Eligibility Nasopharyngeal Carcinoma NCT02460887

    1 Formulieren
    Name
    Type
    Description | Question | Decode (Coded Value)
    Datatype
    Alias
    Item Group
    C1512693 (UMLS CUI)
    Nasopharyngeal Nonkeratinizing Carcinoma
    Item
    patients with newly histologically confirmed non-keratinizing nasopharyngeal carcinoma (including who ii or iii).
    boolean
    C1334926 (UMLS CUI [1])
    AJCC tumor staging
    Item
    tumor staged as t1-4n2-3或t3-4n0-1m0 (according to the 7th ajcc edition).
    boolean
    C0441915 (UMLS CUI [1])
    satisfactory performance status: karnofsky scale
    Item
    satisfactory performance status: karnofsky scale (kps) ≥ 70.
    boolean
    C1520224 (UMLS CUI [1])
    platelet count; hemoglobin
    Item
    adequate marrow: leucocyte count ≥ 4000/μl, hemoglobin ≥ 90g/l and platelet count ≥
    boolean
    C0023508 (UMLS CUI [1])
    C0005821 (UMLS CUI [2])
    C0019046 (UMLS CUI [3])
    alkaline phosphatase; concomitant; normal; liver; upper; ast; uln
    Item
    adequate liver function: alanine aminotransferase (alt), aspartate aminotransferase (ast) < 1.5×upper limit of normal (uln) concomitant with alkaline phosphatase (alp) ≤ 2.5×uln
    boolean
    C0376147 (UMLS CUI [1])
    C0242192 (UMLS CUI [2])
    C0201850 (UMLS CUI [3])
    bilirubin; uln
    Item
    and bilirubin ≤1.5×uln.
    boolean
    C1278039 (UMLS CUI [1])
    creatinine clearance; renal function
    Item
    adequate renal function: creatinine clearance ≥ 60 ml/min.
    boolean
    C0373595 (UMLS CUI [1])
    written informed consent.; study
    Item
    patients must be informed of the investigational nature of this study and give written informed consent.
    boolean
    C0021430 (UMLS CUI [1])
    Item Group
    C0680251 (UMLS CUI)
    Basaloid squamous cell carcinoma | Squamous cell carcinoma, keratinizing
    Item
    who type keratinizing squamous cell carcinoma or basaloid squamous cell carcinoma.
    boolean
    C1266005 (UMLS CUI [1])
    C0334247 (UMLS CUI [2])
    palliative; treatment; intent
    Item
    treatment with palliative intent.
    boolean
    C0087111 (UMLS CUI [1,1])
    C1285530 (UMLS CUI [1,2])
    prior malignancy; cervical; squamous; cancer; skin
    Item
    prior malignancy except adequately treated basal cell or squamous cell skin cancer, in situ cervical cancer.
    boolean
    C0006826 (UMLS CUI [1])
    Patient currently pregnant | Lactating (finding)
    Item
    pregnancy or lactation (consider pregnancy test in women of child-bearing age and emphasize effective contraception during the treatment period).
    boolean
    C0549206 (UMLS CUI [1])
    C2828358 (UMLS CUI [2])
    history of previous rt
    Item
    history of previous rt (except for non-melanomatous skin cancers outside intended rt treatment volume).
    boolean
    C1522449 (UMLS CUI [1])
    prior chemotherapy; primary tumor; surgery; nodes
    Item
    prior chemotherapy or surgery (except diagnostic) to primary tumor or nodes.
    boolean
    C0392920 (UMLS CUI [1])
    C0038894 (UMLS CUI [2,1])
    C0006826 (UMLS CUI [2,2])
    Disease condition determination, uncontrolled | Compliance behavior | Heart Diseases; Unstable status | Kidney Diseases | Hepatitis, Chronic | Diabetes mellitus poor control | Emotional Disturbances
    Item
    any severe intercurrent disease, which may bring unacceptable risk or affect the compliance of the trial, for example, unstable cardiac disease requiring treatment, renal disease, chronic hepatitis, diabetes with poor control (fasting plasma glucose > 1.5×uln), and emotional disturbance.
    boolean
    C0184774 (UMLS CUI [1])
    C1321605 (UMLS CUI [2])
    C0018799 (UMLS CUI [3,1])
    C0443343 (UMLS CUI [3,2])
    C0022658 (UMLS CUI [4])
    C0019189 (UMLS CUI [5])
    C0860161 (UMLS CUI [6])
    C0013985 (UMLS CUI [7])
    Terug naar het begin van de pagina 

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