Information:
Fel:
ID
31016
Beskrivning
A Multicenter Trial Comparing Multi-course Chemotherapy in Locoregionally Advanced Nasopharyngeal Carcinoma; ODM derived from: https://clinicaltrials.gov/show/NCT00705627
Länk
https://clinicaltrials.gov/show/NCT00705627
Nyckelord
Versioner (1)
- 2018-07-10 2018-07-10 -
Rättsinnehavare
See clinicaltrials.gov
Uppladdad den
10 juli 2018
DOI
För en begäran logga in.
Licens
Creative Commons BY 4.0
Modellkommentarer :
Här kan du kommentera modellen. Med hjälp av pratbubblor i Item-grupperna och Item kan du lägga in specifika kommentarer.
Itemgroup-kommentar för :
Item-kommentar för :
Du måste vara inloggad för att kunna ladda ner formulär. Var vänlig logga in eller registrera dig utan kostnad.
Eligibility Nasopharyngeal Carcinoma NCT00705627
Eligibility Nasopharyngeal Carcinoma NCT00705627
- StudyEvent: Eligibility
Similar models
Eligibility Nasopharyngeal Carcinoma NCT00705627
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
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])
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])
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])
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])
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])
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])
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])
Recurrent disease | Distant metastatis
Item
patients have evidence of relapse or distant metastasis
boolean
C0277556 (UMLS CUI [1])
C1269798 (UMLS CUI [2])
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])
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])
C0205394 (UMLS CUI [1,2])
Therapeutic radiology procedure | Chemotherapy
Item
receiving radiotherapy or chemotherapy
boolean
C1522449 (UMLS CUI [1])
C0392920 (UMLS CUI [2])
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])
C2732579 (UMLS CUI [1,2])
C0750558 (UMLS CUI [1,3])