ID

31699

Beschrijving

Study of Neoadjuvant Gemcitabine and Cisplatin in Locoregionally Advanced Nasopharyngeal Carcinoma; ODM derived from: https://clinicaltrials.gov/show/NCT01417390

Link

https://clinicaltrials.gov/show/NCT01417390

Trefwoorden

  1. 21-09-18 21-09-18 -
  2. 21-09-18 21-09-18 - Sarah Riepenhausen
Houder van rechten

First People's Hospital of Foshan

Geüploaded op

21 september 2018

DOI

Voor een aanvraag inloggen.

Licentie

Creative Commons BY-NC 3.0

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Eligibility Nasopharyngeal Carcinoma NCT01417390

Eligibility Nasopharyngeal Carcinoma NCT01417390

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients with newly histologically confirmed non-keratinizing (according to world health organization (who 2005) histologically type).
Beschrijving

Non-keratinizing nasopharyngeal carcinome

Datatype

boolean

Alias
UMLS CUI [1,1]
C1334926
UMLS CUI [1,2]
C1301142
karnofsky scale (kps) > 70.
Beschrijving

Karnofsky Status

Datatype

boolean

Alias
UMLS CUI [1]
C0206065
tumor staged is according to the 7th american joint commission on cancer edition as stage iii:t1-2n2m0, t3n0-2m0 stage iva:t4n0-2m0 stage ivb:any t、n3.
Beschrijving

AJCC Stage

Datatype

boolean

Alias
UMLS CUI [1]
C0441915
adequate marrow: leucocyte count ≥4000/μl, hemoglobin ≥90g/l and platelet count ≥100000/μl.
Beschrijving

Leucocyte count, hemoglobin, platelet count

Datatype

boolean

Alias
UMLS CUI [1]
C0023508
UMLS CUI [2]
C0032181
UMLS CUI [3]
C0518015
UMLS CUI [4]
C0032181
normal liver function test: alanine aminotransferase (alt)、aspartate aminotransferase (ast) <1.5×upper limit of normal (uln) concomitant with alkaline phosphatase (alp) ≤2.5×uln, and bilirubin ≤uln.
Beschrijving

ALT, AST, Alkaline Phosphatase, Bilirubin

Datatype

boolean

Alias
UMLS CUI [1]
C0201836
UMLS CUI [2]
C0201899
UMLS CUI [3]
C0201850
UMLS CUI [4]
C0201913
adequate renal function: creatinine clearance ≥60 ml/min.
Beschrijving

Creatinine clearance

Datatype

boolean

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

Informed consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschrijving

Exclusion Criteria

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

Squamous cell carcinoma

Datatype

boolean

Alias
UMLS CUI [1]
C0007137
age >60 years or <18 years.
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
treatment with palliative intent.
Beschrijving

Palliative intent

Datatype

boolean

Alias
UMLS CUI [1]
C1285530
pregnancy or lactation.
Beschrijving

Pregnancy or lactation

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
prior radiotherapy, chemotherapy or surgery (except diagnostic) to primary tumor or nodes.
Beschrijving

Prior treatment

Datatype

boolean

Alias
UMLS CUI [1]
C1514463
any severe intercurrent disease including unstable cardiac disease, chronic hepatitis, renal disease, diabetes with poor control, and emotional disturbance.
Beschrijving

Comorbidity, including heart disease, chronic hepatitis, renal disease, diabetes and emotional disturbance

Datatype

boolean

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C0205082
UMLS CUI [2,1]
C0018799
UMLS CUI [2,2]
C0205318
UMLS CUI [3]
C0019189
UMLS CUI [4]
C0022658
UMLS CUI [5,1]
C0011849
UMLS CUI [5,2]
C0205318
UMLS CUI [6]
C0013985

Similar models

Eligibility Nasopharyngeal Carcinoma NCT01417390

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Non-keratinizing nasopharyngeal carcinome
Item
patients with newly histologically confirmed non-keratinizing (according to world health organization (who 2005) histologically type).
boolean
C1334926 (UMLS CUI [1,1])
C1301142 (UMLS CUI [1,2])
Karnofsky Status
Item
karnofsky scale (kps) > 70.
boolean
C0206065 (UMLS CUI [1])
AJCC Stage
Item
tumor staged is according to the 7th american joint commission on cancer edition as stage iii:t1-2n2m0, t3n0-2m0 stage iva:t4n0-2m0 stage ivb:any t、n3.
boolean
C0441915 (UMLS CUI [1])
Leucocyte count, hemoglobin, platelet count
Item
adequate marrow: leucocyte count ≥4000/μl, hemoglobin ≥90g/l and platelet count ≥100000/μl.
boolean
C0023508 (UMLS CUI [1])
C0032181 (UMLS CUI [2])
C0518015 (UMLS CUI [3])
C0032181 (UMLS CUI [4])
ALT, AST, Alkaline Phosphatase, Bilirubin
Item
normal liver function test: alanine aminotransferase (alt)、aspartate aminotransferase (ast) <1.5×upper limit of normal (uln) concomitant with alkaline phosphatase (alp) ≤2.5×uln, and bilirubin ≤uln.
boolean
C0201836 (UMLS CUI [1])
C0201899 (UMLS CUI [2])
C0201850 (UMLS CUI [3])
C0201913 (UMLS CUI [4])
Creatinine clearance
Item
adequate renal function: creatinine clearance ≥60 ml/min.
boolean
C0373595 (UMLS CUI [1])
Informed consent
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)
Squamous cell carcinoma
Item
who type keratinizing squamous cell carcinoma.
boolean
C0007137 (UMLS CUI [1])
Age
Item
age >60 years or <18 years.
boolean
C0001779 (UMLS CUI [1])
Palliative intent
Item
treatment with palliative intent.
boolean
C1285530 (UMLS CUI [1])
Pregnancy or lactation
Item
pregnancy or lactation.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Prior treatment
Item
prior radiotherapy, chemotherapy or surgery (except diagnostic) to primary tumor or nodes.
boolean
C1514463 (UMLS CUI [1])
Comorbidity, including heart disease, chronic hepatitis, renal disease, diabetes and emotional disturbance
Item
any severe intercurrent disease including unstable cardiac disease, chronic hepatitis, renal disease, diabetes with poor control, and emotional disturbance.
boolean
C0009488 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0018799 (UMLS CUI [2,1])
C0205318 (UMLS CUI [2,2])
C0019189 (UMLS CUI [3])
C0022658 (UMLS CUI [4])
C0011849 (UMLS CUI [5,1])
C0205318 (UMLS CUI [5,2])
C0013985 (UMLS CUI [6])

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