ID

31016

Description

A Multicenter Trial Comparing Multi-course Chemotherapy in Locoregionally Advanced Nasopharyngeal Carcinoma; ODM derived from: https://clinicaltrials.gov/show/NCT00705627

Link

https://clinicaltrials.gov/show/NCT00705627

Keywords

  1. 7/10/18 7/10/18 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

July 10, 2018

DOI

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License

Creative Commons BY 4.0

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Eligibility Nasopharyngeal Carcinoma NCT00705627

Eligibility Nasopharyngeal Carcinoma NCT00705627

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients with newly histologically confirmed nasopharyngeal carcinoma, including who ii or iii
Description

Nasopharyngeal carcinoma WHO tumor classification Grade

Data type

boolean

Alias
UMLS CUI [1,1]
C2931822
UMLS CUI [1,2]
C1301142
UMLS CUI [1,3]
C0441800
original clinical stage must be t4 or n2-3 (uicc 2002)
Description

TNM clinical staging

Data type

boolean

Alias
UMLS CUI [1]
C3258246
male and no pregnant female
Description

Gender | Pregnancy Absent

Data type

boolean

Alias
UMLS CUI [1]
C0079399
UMLS CUI [2,1]
C0032961
UMLS CUI [2,2]
C0332197
age between 18-60
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
wbc ≥4,000/mm3 and plt ≥ 100,000/mm3
Description

White Blood Cell Count procedure | Platelet Count measurement

Data type

boolean

Alias
UMLS CUI [1]
C0023508
UMLS CUI [2]
C0032181
with normal liver function test (alt、ast≤2.5×uln)
Description

Liver function tests normal | Alanine aminotransferase measurement | Aspartate aminotransferase measurement

Data type

boolean

Alias
UMLS CUI [1]
C0438235
UMLS CUI [2]
C0201836
UMLS CUI [3]
C0201899
with normal renal function test (creatinine ≤ 1.5×uln)
Description

Renal function tests normal | Creatinine measurement, serum

Data type

boolean

Alias
UMLS CUI [1]
C0438262
UMLS CUI [2]
C0201976
performance status scale ecog grade 0,1
Description

ECOG performance status

Data type

boolean

Alias
UMLS CUI [1]
C1520224
without radiotherapy or chemotherapy
Description

Therapeutic radiology procedure Absent | Chemotherapy Absent

Data type

boolean

Alias
UMLS CUI [1,1]
C1522449
UMLS CUI [1,2]
C0332197
UMLS CUI [2,1]
C0392920
UMLS CUI [2,2]
C0332197
patients must give signed informed consent
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients have evidence of relapse or distant metastasis
Description

Recurrent disease | Distant metastatis

Data type

boolean

Alias
UMLS CUI [1]
C0277556
UMLS CUI [2]
C1269798
the presence of uncontrolled life-threatening illness
Description

Life threatening illness Uncontrolled

Data type

boolean

Alias
UMLS CUI [1,1]
C3846017
UMLS CUI [1,2]
C0205318
receiving other ways of anti-cancer therapy
Description

Cancer treatment Other

Data type

boolean

Alias
UMLS CUI [1,1]
C0920425
UMLS CUI [1,2]
C0205394
receiving radiotherapy or chemotherapy
Description

Therapeutic radiology procedure | Chemotherapy

Data type

boolean

Alias
UMLS CUI [1]
C1522449
UMLS CUI [2]
C0392920
investigator consider the patients can't finish the whole study
Description

Patients Completion of clinical trial Unlikely

Data type

boolean

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C2732579
UMLS CUI [1,3]
C0750558

Similar models

Eligibility Nasopharyngeal Carcinoma NCT00705627

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Nasopharyngeal carcinoma WHO tumor classification Grade
Item
patients with newly histologically confirmed nasopharyngeal carcinoma, including who ii or iii
boolean
C2931822 (UMLS CUI [1,1])
C1301142 (UMLS CUI [1,2])
C0441800 (UMLS CUI [1,3])
TNM clinical staging
Item
original clinical stage must be t4 or n2-3 (uicc 2002)
boolean
C3258246 (UMLS CUI [1])
Gender | Pregnancy Absent
Item
male and no pregnant female
boolean
C0079399 (UMLS CUI [1])
C0032961 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
Age
Item
age between 18-60
boolean
C0001779 (UMLS CUI [1])
White Blood Cell Count procedure | Platelet Count measurement
Item
wbc ≥4,000/mm3 and plt ≥ 100,000/mm3
boolean
C0023508 (UMLS CUI [1])
C0032181 (UMLS CUI [2])
Liver function tests normal | Alanine aminotransferase measurement | Aspartate aminotransferase measurement
Item
with normal liver function test (alt、ast≤2.5×uln)
boolean
C0438235 (UMLS CUI [1])
C0201836 (UMLS CUI [2])
C0201899 (UMLS CUI [3])
Renal function tests normal | Creatinine measurement, serum
Item
with normal renal function test (creatinine ≤ 1.5×uln)
boolean
C0438262 (UMLS CUI [1])
C0201976 (UMLS CUI [2])
ECOG performance status
Item
performance status scale ecog grade 0,1
boolean
C1520224 (UMLS CUI [1])
Therapeutic radiology procedure Absent | Chemotherapy Absent
Item
without radiotherapy or chemotherapy
boolean
C1522449 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0392920 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
Informed Consent
Item
patients must give signed informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Recurrent disease | Distant metastatis
Item
patients have evidence of relapse or distant metastasis
boolean
C0277556 (UMLS CUI [1])
C1269798 (UMLS CUI [2])
Life threatening illness Uncontrolled
Item
the presence of uncontrolled life-threatening illness
boolean
C3846017 (UMLS CUI [1,1])
C0205318 (UMLS CUI [1,2])
Cancer treatment Other
Item
receiving other ways of anti-cancer therapy
boolean
C0920425 (UMLS CUI [1,1])
C0205394 (UMLS CUI [1,2])
Therapeutic radiology procedure | Chemotherapy
Item
receiving radiotherapy or chemotherapy
boolean
C1522449 (UMLS CUI [1])
C0392920 (UMLS CUI [2])
Patients Completion of clinical trial Unlikely
Item
investigator consider the patients can't finish the whole study
boolean
C0030705 (UMLS CUI [1,1])
C2732579 (UMLS CUI [1,2])
C0750558 (UMLS CUI [1,3])

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