Informações:
Falhas:
ID
15758
Descrição
Trial Comparing Two Strategies of Chemotherapy for Metastatic Colorectal Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00126256
Link
https://clinicaltrials.gov/show/NCT00126256
Palavras-chave
Versões (1)
- 11/06/2016 11/06/2016 -
Transferido a
11 de junho de 2016
DOI
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Licença
Creative Commons BY 4.0
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Eligibility Colorectal Cancer NCT00126256
Eligibility Colorectal Cancer NCT00126256
- StudyEvent: Eligibility
Similar models
Eligibility Colorectal Cancer NCT00126256
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
metastatic colorectal adenocarcinoma
Item
histologically confirmed metastatic colorectal adenocarcinoma
boolean
C1319315 (UMLS CUI [1,1])
C0027627 (UMLS CUI [1,2])
C0027627 (UMLS CUI [1,2])
unresectable metastasis
Item
unresectable metastasis
boolean
C0027627 (UMLS CUI [1,1])
C1519810 (UMLS CUI [1,2])
C1519810 (UMLS CUI [1,2])
bidimensionally measurable disease
Item
bidimensionally measurable disease (world health organization [who] criteria)
boolean
C1513041 (UMLS CUI [1])
WHO performance status
Item
who performance status of 2 or less
boolean
C1298650 (UMLS CUI [1])
hematologic functions
Item
adequate hematologic functions (neutrophil count, at least 1500 per cubic millimeter; and platelet count, at least 100,000 per cubic millimetre)
boolean
C0200633 (UMLS CUI [1])
C0005821 (UMLS CUI [2])
C0005821 (UMLS CUI [2])
renal function
Item
adequate renal function (serum creatinine, less than 125 micromol per liter)
boolean
C0201976 (UMLS CUI [1])
liver function
Item
adequate liver function (bilirubin, not more than 5 times the upper limit of normal)
boolean
C1278039 (UMLS CUI [1])
no previous chemotherapy
Item
no previous chemotherapy other than previous adjuvant chemotherapy or concomitant chemoradiotherapy with 5-fluorouracil and leucovorin for the treatment of the primary tumor completed at least 6 months before inclusion
boolean
C0392920 (UMLS CUI [1])
written inform consent
Item
signed written inform consent
boolean
C0021430 (UMLS CUI [1])
quality of life questionnaire
Item
quality of life questionnaire (qlq c-30) filled out
boolean
C0518214 (UMLS CUI [1])
pregnancy or breast-feeding
Item
pregnant or breast – feeding women
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0006147 (UMLS CUI [2])
impossibility of regular follow-up
Item
impossibility of regular follow-up for psychological, social or geographical reason
boolean
C0814423 (UMLS CUI [1,1])
C1522577 (UMLS CUI [1,2])
C1522577 (UMLS CUI [1,2])
severe organ failure
Item
severe cardiac, respiratory, renal or hepatic failure
boolean
C0009488 (UMLS CUI [1])
coronary heart disease
Item
active coronary heart disease
boolean
C0010068 (UMLS CUI [1])
psychological illness
Item
patients with a history of a psychological illness or condition such as to interfere with the patient’s ability to understand the requirements of the study
boolean
C0004936 (UMLS CUI [1])
C0004936 (UMLS CUI [2,1])
C1321605 (UMLS CUI [2,2])
C0439801 (UMLS CUI [2,3])
C0004936 (UMLS CUI [2,1])
C1321605 (UMLS CUI [2,2])
C0439801 (UMLS CUI [2,3])
CNS metastases
Item
central nervous system metastases
boolean
C0686377 (UMLS CUI [1])
history of second malignancies
Item
past history of second malignancies
boolean
C0006826 (UMLS CUI [1])
another investigational drug
Item
another investigational drug
boolean
C2348568 (UMLS CUI [1])
chronic inflammatory bowel disease
Item
chronic inflammatory bowel disease
boolean
C1856359 (UMLS CUI [1])
chemotherapy with irinotecan or oxaliplatin
Item
previous chemotherapy with irinotecan or oxaliplatin based regimens
boolean
C0392920 (UMLS CUI [1,1])
C0123931 (UMLS CUI [1,2])
C0392920 (UMLS CUI [2,1])
C0069717 (UMLS CUI [2,2])
C0123931 (UMLS CUI [1,2])
C0392920 (UMLS CUI [2,1])
C0069717 (UMLS CUI [2,2])