ID

28301

Description

Standard Versus Advanced Antimicrobial Dressing Containing Ionic Silver Following Colorectal Cancer Surgery; ODM derived from: https://clinicaltrials.gov/show/NCT00981110

Link

https://clinicaltrials.gov/show/NCT00981110

Keywords

  1. 1/3/18 1/3/18 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

January 3, 2018

DOI

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License

Creative Commons BY 4.0

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Eligibility Colorectal Cancer NCT00981110

Eligibility Colorectal Cancer NCT00981110

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

Data type

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

Data type

boolean

Alias
UMLS CUI [1]
C0001779
informed signed consent
Description

Informed Consent

Data type

boolean

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

ECOG performance status

Data type

boolean

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

Platelet Count measurement

Data type

boolean

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

Prothrombin time

Data type

boolean

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

White Blood Cell Count procedure

Data type

boolean

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

Life Expectancy

Data type

boolean

Alias
UMLS CUI [1]
C0023671
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
intestinal obstruction
Description

Intestinal Obstruction

Data type

boolean

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

Intestinal hemorrhage Severe | Blood Transfusion Patient need for

Data type

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

Data type

boolean

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

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

Data type

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

Data type

boolean

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

Communicable Diseases

Data type

boolean

Alias
UMLS CUI [1]
C0009450
coagulopathy
Description

Blood Coagulation Disorder

Data type

boolean

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

Informed Consent Unable

Data type

boolean

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

Hypersensitivity Dressing Component

Data type

boolean

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

Similar models

Eligibility Colorectal Cancer NCT00981110

Name
Type
Description | Question | Decode (Coded Value)
Data type
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])

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