Eligibility LOCALLY ADVANCED UNDIFFERENTIATED CARCINOMA NASOPHARYNGEAL TYPE UCNT NCT00180973

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
of either sex
Description

Gender

Type de données

boolean

Alias
UMLS CUI [1]
C0079399
aged 15 to 70 years
Description

Age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
never previously treated with radiotherapy, chemotherapy or surgery for malignant disease (except neck adenectomy/diagnosis)
Description

ID.3

Type de données

boolean

Alias
UMLS CUI [1]
C0087111
UMLS CUI [2]
C1522449
UMLS CUI [3]
C0392920
UMLS CUI [4]
C0038894
with awho performance status * 2.
Description

who performance

Type de données

boolean

Alias
UMLS CUI [1]
C1298650
amenable to regular follow-up
Description

follow-up

Type de données

boolean

Alias
UMLS CUI [1]
C1321605
capable of receiving chemotherapy and radiotherapy : in particular, with no contraindications to the use of anthracyclines, bleomycin or cisplatinum.
Description

capable of receiving therapy

Type de données

boolean

Alias
UMLS CUI [1]
C1321605
with informed consent at entry time, in writing or witnessed oral informed consent, in accordance with local legislation requirements.
Description

informed consent

Type de données

boolean

Alias
UMLS CUI [1]
C0021430
neutrophil count * 2000 /mm3 platelet count * 150,000 /mm3 hemoglobin * 10 g / dl
Description

Laboratory results

Type de données

boolean

Alias
UMLS CUI [1]
C0200633
UMLS CUI [2]
C0005821
UMLS CUI [3]
C0019046
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
histologic types other than type ii - iii of the who classification
Description

histology

Type de données

boolean

Alias
UMLS CUI [1]
C0449574
t1 - t2 n0 - n1 or patients with metastatic
Description

Tumor stage

Type de données

boolean

Alias
UMLS CUI [1]
C1300072
aged < 15 or > 70.
Description

Age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
patients in whom chemotherapy is contraindicated: history of myocardial infarction over the last 6 months before inclusion, or clinically present cardiac pathology.
Description

contraindication chemotherapy, myocardial infarcion, heart diseases

Type de données

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0392920
UMLS CUI [2]
C0027051
UMLS CUI [3]
C0018799
who performance status >2
Description

who performance

Type de données

boolean

Alias
UMLS CUI [1]
C1298650
history of prior malignancies (other than non melanoma skin cancer or excised cervical carcinoma in situ).
Description

prior malignancies

Type de données

boolean

Alias
UMLS CUI [1]
C0006826
uncontrolled infection,
Description

uncontrolled infection

Type de données

boolean

Alias
UMLS CUI [1]
C0009488
patients refusing participation.
Description

refusing participation

Type de données

boolean

Alias
UMLS CUI [1]
C1321605
patients who, for social, familial or geographic reasons are unlikely to comply with a long term follow-up.
Description

unlikely to comply with a long term follow-up

Type de données

boolean

Alias
UMLS CUI [1]
C1321605

Similar models

Eligibility LOCALLY ADVANCED UNDIFFERENTIATED CARCINOMA NASOPHARYNGEAL TYPE UCNT NCT00180973

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Gender
Item
of either sex
boolean
C0079399 (UMLS CUI [1])
Age
Item
aged 15 to 70 years
boolean
C0001779 (UMLS CUI [1])
ID.3
Item
never previously treated with radiotherapy, chemotherapy or surgery for malignant disease (except neck adenectomy/diagnosis)
boolean
C0087111 (UMLS CUI [1])
C1522449 (UMLS CUI [2])
C0392920 (UMLS CUI [3])
C0038894 (UMLS CUI [4])
who performance
Item
with awho performance status * 2.
boolean
C1298650 (UMLS CUI [1])
follow-up
Item
amenable to regular follow-up
boolean
C1321605 (UMLS CUI [1])
capable of receiving therapy
Item
capable of receiving chemotherapy and radiotherapy : in particular, with no contraindications to the use of anthracyclines, bleomycin or cisplatinum.
boolean
C1321605 (UMLS CUI [1])
informed consent
Item
with informed consent at entry time, in writing or witnessed oral informed consent, in accordance with local legislation requirements.
boolean
C0021430 (UMLS CUI [1])
Laboratory results
Item
neutrophil count * 2000 /mm3 platelet count * 150,000 /mm3 hemoglobin * 10 g / dl
boolean
C0200633 (UMLS CUI [1])
C0005821 (UMLS CUI [2])
C0019046 (UMLS CUI [3])
Item Group
C0680251 (UMLS CUI)
histology
Item
histologic types other than type ii - iii of the who classification
boolean
C0449574 (UMLS CUI [1])
Tumor stage
Item
t1 - t2 n0 - n1 or patients with metastatic
boolean
C1300072 (UMLS CUI [1])
Age
Item
aged < 15 or > 70.
boolean
C0001779 (UMLS CUI [1])
contraindication chemotherapy, myocardial infarcion, heart diseases
Item
patients in whom chemotherapy is contraindicated: history of myocardial infarction over the last 6 months before inclusion, or clinically present cardiac pathology.
boolean
C1301624 (UMLS CUI [1,1])
C0392920 (UMLS CUI [1,2])
C0027051 (UMLS CUI [2])
C0018799 (UMLS CUI [3])
who performance
Item
who performance status >2
boolean
C1298650 (UMLS CUI [1])
prior malignancies
Item
history of prior malignancies (other than non melanoma skin cancer or excised cervical carcinoma in situ).
boolean
C0006826 (UMLS CUI [1])
uncontrolled infection
Item
uncontrolled infection,
boolean
C0009488 (UMLS CUI [1])
refusing participation
Item
patients refusing participation.
boolean
C1321605 (UMLS CUI [1])
unlikely to comply with a long term follow-up
Item
patients who, for social, familial or geographic reasons are unlikely to comply with a long term follow-up.
boolean
C1321605 (UMLS CUI [1])