Anglais

Eligibility Colorectal Cancer NCT00981110

1 Formulaires  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients bearing solid tumours who are candidate to open radical surgery for colorectal cancer (histology proven)
Description

Solid tumour | Patient Schedule | Operative Surgical Procedure Radical Colorectal Carcinoma

Type de données

boolean

Alias
UMLS CUI [1]
C0280100
UMLS CUI [2]
C0030703
UMLS CUI [3,1]
C0543467
UMLS CUI [3,2]
C0439807
UMLS CUI [3,3]
C0009402
age 18-75
Description

Age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
informed signed consent
Description

Informed Consent

Type de données

boolean

Alias
UMLS CUI [1]
C0021430
performance status 0-2 (according to ecog score)
Description

ECOG performance status

Type de données

boolean

Alias
UMLS CUI [1]
C1520224
platelets > 50.000/mm3
Description

Platelet Count measurement

Type de données

boolean

Alias
UMLS CUI [1]
C0032181
prothrombin time (quick) > 60%
Description

Prothrombin time

Type de données

boolean

Alias
UMLS CUI [1]
C0033707
white blood cells > 2500/mm3
Description

White Blood Cell Count procedure

Type de données

boolean

Alias
UMLS CUI [1]
C0023508
life expectancy > 3 months
Description

Life Expectancy

Type de données

boolean

Alias
UMLS CUI [1]
C0023671
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
intestinal obstruction
Description

Intestinal Obstruction

Type de données

boolean

Alias
UMLS CUI [1]
C0021843
severe intestinal bleeding requiring blood transfusion
Description

Intestinal hemorrhage Severe | Blood Transfusion Patient need for

Type de données

boolean

Alias
UMLS CUI [1,1]
C0267373
UMLS CUI [1,2]
C0205082
UMLS CUI [2,1]
C0005841
UMLS CUI [2,2]
C0686904
age under 18 or over 75
Description

Age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
severe hepatic failure (ascites, portal hypertension, jaundice or encephalopathy)
Description

Liver Failure Severe | Ascites | Hypertension, Portal | Icterus | Encephalopathy

Type de données

boolean

Alias
UMLS CUI [1,1]
C0085605
UMLS CUI [1,2]
C0205082
UMLS CUI [2]
C0003962
UMLS CUI [3]
C0020541
UMLS CUI [4]
C0022346
UMLS CUI [5]
C0085584
renal failure (hemodialysis, creatinin > 2.5 mg/dl)
Description

Kidney Failure | Hemodialysis | Creatinine measurement, serum

Type de données

boolean

Alias
UMLS CUI [1]
C0035078
UMLS CUI [2]
C0019004
UMLS CUI [3]
C0201976
active infections
Description

Communicable Diseases

Type de données

boolean

Alias
UMLS CUI [1]
C0009450
coagulopathy
Description

Blood Coagulation Disorder

Type de données

boolean

Alias
UMLS CUI [1]
C0005779
inability to give an informed consent
Description

Informed Consent Unable

Type de données

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1299582
known allergies to dressing components
Description

Hypersensitivity Dressing Component

Type de données

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0013119
UMLS CUI [1,3]
C1705248
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Similar models

Eligibility Colorectal Cancer NCT00981110

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Solid tumour | Patient Schedule | Operative Surgical Procedure Radical Colorectal Carcinoma
Item
patients bearing solid tumours who are candidate to open radical surgery for colorectal cancer (histology proven)
boolean
C0280100 (UMLS CUI [1])
C0030703 (UMLS CUI [2])
C0543467 (UMLS CUI [3,1])
C0439807 (UMLS CUI [3,2])
C0009402 (UMLS CUI [3,3])
Age
Item
age 18-75
boolean
C0001779 (UMLS CUI [1])
Informed Consent
Item
informed signed consent
boolean
C0021430 (UMLS CUI [1])
ECOG performance status
Item
performance status 0-2 (according to ecog score)
boolean
C1520224 (UMLS CUI [1])
Platelet Count measurement
Item
platelets > 50.000/mm3
boolean
C0032181 (UMLS CUI [1])
Prothrombin time
Item
prothrombin time (quick) > 60%
boolean
C0033707 (UMLS CUI [1])
White Blood Cell Count procedure
Item
white blood cells > 2500/mm3
boolean
C0023508 (UMLS CUI [1])
Life Expectancy
Item
life expectancy > 3 months
boolean
C0023671 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Intestinal Obstruction
Item
intestinal obstruction
boolean
C0021843 (UMLS CUI [1])
Intestinal hemorrhage Severe | Blood Transfusion Patient need for
Item
severe intestinal bleeding requiring blood transfusion
boolean
C0267373 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0005841 (UMLS CUI [2,1])
C0686904 (UMLS CUI [2,2])
Age
Item
age under 18 or over 75
boolean
C0001779 (UMLS CUI [1])
Liver Failure Severe | Ascites | Hypertension, Portal | Icterus | Encephalopathy
Item
severe hepatic failure (ascites, portal hypertension, jaundice or encephalopathy)
boolean
C0085605 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0003962 (UMLS CUI [2])
C0020541 (UMLS CUI [3])
C0022346 (UMLS CUI [4])
C0085584 (UMLS CUI [5])
Kidney Failure | Hemodialysis | Creatinine measurement, serum
Item
renal failure (hemodialysis, creatinin > 2.5 mg/dl)
boolean
C0035078 (UMLS CUI [1])
C0019004 (UMLS CUI [2])
C0201976 (UMLS CUI [3])
Communicable Diseases
Item
active infections
boolean
C0009450 (UMLS CUI [1])
Blood Coagulation Disorder
Item
coagulopathy
boolean
C0005779 (UMLS CUI [1])
Informed Consent Unable
Item
inability to give an informed consent
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
Hypersensitivity Dressing Component
Item
known allergies to dressing components
boolean
C0020517 (UMLS CUI [1,1])
C0013119 (UMLS CUI [1,2])
C1705248 (UMLS CUI [1,3])
Retour au début de la page