ID

12215

Description

DC-CIK Combined With TACE in the Treatment of Hepatocellular Carcinoma; ODM derived from: https://clinicaltrials.gov/show/NCT02487017

Link

https://clinicaltrials.gov/show/NCT02487017

Keywords

  1. 10/18/15 10/18/15 -
Uploaded on

October 18, 2015

DOI

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License

Creative Commons BY 4.0

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Eligibility Hepatocellular Carcinoma NCT02487017

Eligibility Hepatocellular Carcinoma NCT02487017

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
18-80 years old;
Description

age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
histologically confirmed with hepatocellular carcinoma at stage i-ii;
Description

hepatocellular carcinoma

Data type

boolean

Alias
UMLS CUI [1]
C2239176
patients who can accept transcatheter arterial chemoembolization ;
Description

Transarterial Chemoembolization

Data type

boolean

Alias
UMLS CUI [1]
C3539919
patients who have a life expectancy of at least 3 months;
Description

life expectancy

Data type

boolean

Alias
UMLS CUI [1]
C0023671
patients who have a child-pugh:a/b; .eastern cooperative oncology group (ecog) performance status was 0-2.
Description

ecog performance status

Data type

boolean

Alias
UMLS CUI [1]
C1520224
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
white blood cell <3 x 10^9/l,platelet count <75 x 10^9/l;bun and cr more than normal limits on 3.0 times ;
Description

Blood Platelets; white blood cell

Data type

boolean

Alias
UMLS CUI [1]
C0005821
UMLS CUI [2]
C0023516
known or suspected allergy to the investigational agent or any agent given in association with this trial;
Description

allergy

Data type

boolean

Alias
UMLS CUI [1]
C0020517
pregnant or lactating patients;
Description

pregnant; lactating

Data type

boolean

Alias
UMLS CUI [1]
C0549206
UMLS CUI [2]
C2828358
known history of human immunodeficiency virus (hiv), hepatitis c virus (hcv) or treponemapallidun (tp) infection;
Description

human immunodeficiency virus (hiv) infection; hepatitis c virus (hcv)

Data type

boolean

Alias
UMLS CUI [1]
C0019693
UMLS CUI [2]
C0220847
patients who are suffering from serious autoimmune disease;
Description

autoimmune disease

Data type

boolean

Alias
UMLS CUI [1]
C0004364
patients who had used long time or are using immunosuppressant;
Description

immunosuppressant

Data type

boolean

Alias
UMLS CUI [1]
C0021081
patients who had active infection;
Description

infection; active

Data type

boolean

Alias
UMLS CUI [1]
C3714514
UMLS CUI [2]
C0205177
prior use of any anti-cancer treatment in 30 days;
Description

cancer treatment

Data type

boolean

Alias
UMLS CUI [1]
C0920425
now or recently will join another experimental clinical study ;
Description

clinical study

Data type

boolean

Alias
UMLS CUI [1]
C0008972
history of organ allograft;
Description

organ; allograft

Data type

boolean

Alias
UMLS CUI [1]
C0178784
UMLS CUI [2]
C0040739
other situations that the researchers considered unsuitable for this study
Description

Clinical Research; Disruption

Data type

boolean

Alias
UMLS CUI [1]
C0008972
UMLS CUI [2]
C0332453

Similar models

Eligibility Hepatocellular Carcinoma NCT02487017

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
age
Item
18-80 years old;
boolean
C0001779 (UMLS CUI [1])
hepatocellular carcinoma
Item
histologically confirmed with hepatocellular carcinoma at stage i-ii;
boolean
C2239176 (UMLS CUI [1])
Transarterial Chemoembolization
Item
patients who can accept transcatheter arterial chemoembolization ;
boolean
C3539919 (UMLS CUI [1])
life expectancy
Item
patients who have a life expectancy of at least 3 months;
boolean
C0023671 (UMLS CUI [1])
ecog performance status
Item
patients who have a child-pugh:a/b; .eastern cooperative oncology group (ecog) performance status was 0-2.
boolean
C1520224 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Blood Platelets; white blood cell
Item
white blood cell <3 x 10^9/l,platelet count <75 x 10^9/l;bun and cr more than normal limits on 3.0 times ;
boolean
C0005821 (UMLS CUI [1])
C0023516 (UMLS CUI [2])
allergy
Item
known or suspected allergy to the investigational agent or any agent given in association with this trial;
boolean
C0020517 (UMLS CUI [1])
pregnant; lactating
Item
pregnant or lactating patients;
boolean
C0549206 (UMLS CUI [1])
C2828358 (UMLS CUI [2])
human immunodeficiency virus (hiv) infection; hepatitis c virus (hcv)
Item
known history of human immunodeficiency virus (hiv), hepatitis c virus (hcv) or treponemapallidun (tp) infection;
boolean
C0019693 (UMLS CUI [1])
C0220847 (UMLS CUI [2])
autoimmune disease
Item
patients who are suffering from serious autoimmune disease;
boolean
C0004364 (UMLS CUI [1])
immunosuppressant
Item
patients who had used long time or are using immunosuppressant;
boolean
C0021081 (UMLS CUI [1])
infection; active
Item
patients who had active infection;
boolean
C3714514 (UMLS CUI [1])
C0205177 (UMLS CUI [2])
cancer treatment
Item
prior use of any anti-cancer treatment in 30 days;
boolean
C0920425 (UMLS CUI [1])
clinical study
Item
now or recently will join another experimental clinical study ;
boolean
C0008972 (UMLS CUI [1])
organ; allograft
Item
history of organ allograft;
boolean
C0178784 (UMLS CUI [1])
C0040739 (UMLS CUI [2])
Clinical Research; Disruption
Item
other situations that the researchers considered unsuitable for this study
boolean
C0008972 (UMLS CUI [1])
C0332453 (UMLS CUI [2])

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