Information:
Fel:
ID
41138
Beskrivning
Analysis of Body Composition in Patients With Hepatocellular Carcinoma in Radioablation; ODM derived from: https://clinicaltrials.gov/show/NCT01744639
Länk
https://clinicaltrials.gov/show/NCT01744639
Nyckelord
Versioner (1)
- 2020-06-29 2020-06-29 -
Rättsinnehavare
See clinicaltrials.gov
Uppladdad den
29 juni 2020
DOI
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Licens
Creative Commons BY 4.0
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Eligibility Liver Carcinoma NCT01744639
Eligibility Liver Carcinoma NCT01744639
- StudyEvent: Eligibility
Similar models
Eligibility Liver Carcinoma NCT01744639
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
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])
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])
C0600109 (UMLS CUI [1,2])
Liver disease | Kidney Disease
Item
patients with hepato-renal diseases.
boolean
C0023895 (UMLS CUI [1])
C0022658 (UMLS CUI [2])
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])
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])
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])
C0558080 (UMLS CUI [1,2])
Tests Incomplete
Item
incomplete applied tests
boolean
C0022885 (UMLS CUI [1,1])
C0205257 (UMLS CUI [1,2])
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])
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])
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])
C0011065 (UMLS CUI [2])
C0231290 (UMLS CUI [3,1])
C0850292 (UMLS CUI [3,2])
C0205435 (UMLS CUI [3,3])