ID

41138

Description

Analysis of Body Composition in Patients With Hepatocellular Carcinoma in Radioablation; ODM derived from: https://clinicaltrials.gov/show/NCT01744639

Link

https://clinicaltrials.gov/show/NCT01744639

Keywords

Versions (1)
  1. 6/29/20 6/29/20 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

June 29, 2020

DOI

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License

Creative Commons BY 4.0
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Eligibility Liver Carcinoma NCT01744639

English

Eligibility Liver Carcinoma NCT01744639

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients with a diagnosis of hepatocellular carcinoma, treatment-naive and who are referred to the radiology department for radioablation as first therapy.
Description

Liver carcinoma | Therapy naive | Referral for Radiofrequency Ablation First line treatment

Data type

boolean

Alias
UMLS CUI [1]
C2239176
UMLS CUI [2]
C0919936
UMLS CUI [3,1]
C2585524
UMLS CUI [3,2]
C0850292
UMLS CUI [3,3]
C1708063
outpatients.
Description

Outpatients

Data type

boolean

Alias
UMLS CUI [1]
C0029921
willingness to participate in the project.
Description

Study Subject Participation Status Willing

Data type

boolean

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C0600109
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients with hepato-renal diseases.
Description

Liver disease | Kidney Disease

Data type

boolean

Alias
UMLS CUI [1]
C0023895
UMLS CUI [2]
C0022658
patients diagnosed with hepatocellular carcinoma undergoing chemoembolization treatment, or who have received more than one session radioablation.
Description

Liver carcinoma | Chemoembolization, Therapeutic | Radiofrequency Ablation Quantity

Data type

boolean

Alias
UMLS CUI [1]
C2239176
UMLS CUI [2]
C0085075
UMLS CUI [3,1]
C0850292
UMLS CUI [3,2]
C1265611
patients with depression or psychiatric illnesses
Description

Depressive disorder | Mental disorders

Data type

boolean

Alias
UMLS CUI [1]
C0011581
UMLS CUI [2]
C0004936
patients who do not agree to participate in the project.
Description

Study Subject Participation Status Unwilling

Data type

boolean

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C0558080
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
incomplete applied tests
Description

Tests Incomplete

Data type

boolean

Alias
UMLS CUI [1,1]
C0022885
UMLS CUI [1,2]
C0205257
disagreement of the person to perform any of the tests
Description

Tests Perform Unwilling

Data type

boolean

Alias
UMLS CUI [1,1]
C0022885
UMLS CUI [1,2]
C0884358
UMLS CUI [1,3]
C0558080
monitoring breach
Description

Monitoring Failed

Data type

boolean

Alias
UMLS CUI [1,1]
C0030695
UMLS CUI [1,2]
C0231175
hospitalization or death after the first session radioablation.
Description

Hospitalization | Death | Status post Radiofrequency Ablation First

Data type

boolean

Alias
UMLS CUI [1]
C0019993
UMLS CUI [2]
C0011065
UMLS CUI [3,1]
C0231290
UMLS CUI [3,2]
C0850292
UMLS CUI [3,3]
C0205435
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Similar models

Eligibility Liver Carcinoma NCT01744639

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Liver carcinoma | Therapy naive | Referral for Radiofrequency Ablation First line treatment
Item
patients with a diagnosis of hepatocellular carcinoma, treatment-naive and who are referred to the radiology department for radioablation as first therapy.
boolean
C2239176 (UMLS CUI [1])
C0919936 (UMLS CUI [2])
C2585524 (UMLS CUI [3,1])
C0850292 (UMLS CUI [3,2])
C1708063 (UMLS CUI [3,3])
Outpatients
Item
outpatients.
boolean
C0029921 (UMLS CUI [1])
Study Subject Participation Status Willing
Item
willingness to participate in the project.
boolean
C2348568 (UMLS CUI [1,1])
C0600109 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Liver disease | Kidney Disease
Item
patients with hepato-renal diseases.
boolean
C0023895 (UMLS CUI [1])
C0022658 (UMLS CUI [2])
Liver carcinoma | Chemoembolization, Therapeutic | Radiofrequency Ablation Quantity
Item
patients diagnosed with hepatocellular carcinoma undergoing chemoembolization treatment, or who have received more than one session radioablation.
boolean
C2239176 (UMLS CUI [1])
C0085075 (UMLS CUI [2])
C0850292 (UMLS CUI [3,1])
C1265611 (UMLS CUI [3,2])
Depressive disorder | Mental disorders
Item
patients with depression or psychiatric illnesses
boolean
C0011581 (UMLS CUI [1])
C0004936 (UMLS CUI [2])
Study Subject Participation Status Unwilling
Item
patients who do not agree to participate in the project.
boolean
C2348568 (UMLS CUI [1,1])
C0558080 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Tests Incomplete
Item
incomplete applied tests
boolean
C0022885 (UMLS CUI [1,1])
C0205257 (UMLS CUI [1,2])
Tests Perform Unwilling
Item
disagreement of the person to perform any of the tests
boolean
C0022885 (UMLS CUI [1,1])
C0884358 (UMLS CUI [1,2])
C0558080 (UMLS CUI [1,3])
Monitoring Failed
Item
monitoring breach
boolean
C0030695 (UMLS CUI [1,1])
C0231175 (UMLS CUI [1,2])
Hospitalization | Death | Status post Radiofrequency Ablation First
Item
hospitalization or death after the first session radioablation.
boolean
C0019993 (UMLS CUI [1])
C0011065 (UMLS CUI [2])
C0231290 (UMLS CUI [3,1])
C0850292 (UMLS CUI [3,2])
C0205435 (UMLS CUI [3,3])
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