Informatie:
Fout:
ID
44348
Beschrijving
Magnetic Resonance Elastography (MRE) as a Predictor of HCC Recurrence After Radiofrequency Ablation (RFA); ODM derived from: https://clinicaltrials.gov/show/NCT01447667
Link
https://clinicaltrials.gov/show/NCT01447667
Trefwoorden
Versies (2)
- 26-01-20 26-01-20 -
- 20-09-21 20-09-21 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
20 september 2021
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Hepatic Fibrosis NCT01447667
Eligibility Hepatic Fibrosis NCT01447667
- StudyEvent: Eligibility
Similar models
Eligibility Hepatic Fibrosis NCT01447667
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Liver carcinoma hypervascular single
Item
diagnosed as single hypervascular hepatocellular carcinoma initially
boolean
C2239176 (UMLS CUI [1,1])
C1512560 (UMLS CUI [1,2])
C0205171 (UMLS CUI [1,3])
C1512560 (UMLS CUI [1,2])
C0205171 (UMLS CUI [1,3])
Liver carcinoma TNM clinical staging
Item
ajcc stage i hcc
boolean
C2239176 (UMLS CUI [1,1])
C3258246 (UMLS CUI [1,2])
C3258246 (UMLS CUI [1,2])
Child-Pugh Classification
Item
child-pugh class a
boolean
C4050412 (UMLS CUI [1])
Radiofrequency ablation Liver carcinoma Planned
Item
planning radiofrequency ablation for hcc
boolean
C0850292 (UMLS CUI [1,1])
C2239176 (UMLS CUI [1,2])
C1301732 (UMLS CUI [1,3])
C2239176 (UMLS CUI [1,2])
C1301732 (UMLS CUI [1,3])
Agreement Voluntary Clinical Trial
Item
voluntary agreement for this study
boolean
C0680240 (UMLS CUI [1,1])
C0439656 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
C0439656 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
Decreased renal function | Glomerular Filtration Rate
Item
decreased kidney function (gfr < 70 ml/min/kg)
boolean
C0232807 (UMLS CUI [1])
C0017654 (UMLS CUI [2])
C0017654 (UMLS CUI [2])
Medical contraindication MRI | Pacemaker | Defibrillator
Item
contraindication to mri (pacemaker, defibrillator)
boolean
C1301624 (UMLS CUI [1,1])
C0024485 (UMLS CUI [1,2])
C0810633 (UMLS CUI [2])
C0180307 (UMLS CUI [3])
C0024485 (UMLS CUI [1,2])
C0810633 (UMLS CUI [2])
C0180307 (UMLS CUI [3])
Contrast media allergy
Item
contrast media hypersensitivity
boolean
C0570562 (UMLS CUI [1])
Primary tumor Other
Item
other primary malignancy
boolean
C0677930 (UMLS CUI [1,1])
C0205394 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,2])
Viral hepatitis
Item
acute viral hepatitis
boolean
C0042721 (UMLS CUI [1])
Transplantation of liver
Item
prior history of liver transplantation
boolean
C0023911 (UMLS CUI [1])
Splenic vein thrombosis | Portal vein thrombosis
Item
thrombosis in splenic vein or portal vein
boolean
C0272416 (UMLS CUI [1])
C0155773 (UMLS CUI [2])
C0155773 (UMLS CUI [2])
Study Subject Participation Status | Clinical Trials
Item
patients who were enrolled to other clinical trials within 4 weeks
boolean
C2348568 (UMLS CUI [1])
C0008976 (UMLS CUI [2])
C0008976 (UMLS CUI [2])
Chronic disease Severe | Mental Disorder, Severe
Item
other severe chronic disease or psychiatric disease
boolean
C0008679 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C4046029 (UMLS CUI [2])
C0205082 (UMLS CUI [1,2])
C4046029 (UMLS CUI [2])
Pregnancy | Breast Feeding
Item
pregnant or milk-feeding women
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0006147 (UMLS CUI [2])
Blood Coagulation Disorders | High risk of bleeding Biopsy of liver
Item
patients with coagulopathy, high risk of bleeding for the liver biopsy
boolean
C0005779 (UMLS CUI [1])
C4039184 (UMLS CUI [2,1])
C0193388 (UMLS CUI [2,2])
C4039184 (UMLS CUI [2,1])
C0193388 (UMLS CUI [2,2])
Study Subject Participation Status Disagreement
Item
patients who disagree to participate in this study
boolean
C2348568 (UMLS CUI [1,1])
C0680238 (UMLS CUI [1,2])
C0680238 (UMLS CUI [1,2])