ID

44348

Beskrivning

Magnetic Resonance Elastography (MRE) as a Predictor of HCC Recurrence After Radiofrequency Ablation (RFA); ODM derived from: https://clinicaltrials.gov/show/NCT01447667

Länk

https://clinicaltrials.gov/show/NCT01447667

Nyckelord

  1. 2020-01-26 2020-01-26 -
  2. 2021-09-20 2021-09-20 -
Rättsinnehavare

See clinicaltrials.gov

Uppladdad den

20 september 2021

DOI

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Licens

Creative Commons BY 4.0

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Eligibility Hepatic Fibrosis NCT01447667

Eligibility Hepatic Fibrosis NCT01447667

Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
diagnosed as single hypervascular hepatocellular carcinoma initially
Beskrivning

Liver carcinoma hypervascular single

Datatyp

boolean

Alias
UMLS CUI [1,1]
C2239176
UMLS CUI [1,2]
C1512560
UMLS CUI [1,3]
C0205171
ajcc stage i hcc
Beskrivning

Liver carcinoma TNM clinical staging

Datatyp

boolean

Alias
UMLS CUI [1,1]
C2239176
UMLS CUI [1,2]
C3258246
child-pugh class a
Beskrivning

Child-Pugh Classification

Datatyp

boolean

Alias
UMLS CUI [1]
C4050412
planning radiofrequency ablation for hcc
Beskrivning

Radiofrequency ablation Liver carcinoma Planned

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0850292
UMLS CUI [1,2]
C2239176
UMLS CUI [1,3]
C1301732
voluntary agreement for this study
Beskrivning

Agreement Voluntary Clinical Trial

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0680240
UMLS CUI [1,2]
C0439656
UMLS CUI [1,3]
C0008976
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
decreased kidney function (gfr < 70 ml/min/kg)
Beskrivning

Decreased renal function | Glomerular Filtration Rate

Datatyp

boolean

Alias
UMLS CUI [1]
C0232807
UMLS CUI [2]
C0017654
contraindication to mri (pacemaker, defibrillator)
Beskrivning

Medical contraindication MRI | Pacemaker | Defibrillator

Datatyp

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0024485
UMLS CUI [2]
C0810633
UMLS CUI [3]
C0180307
contrast media hypersensitivity
Beskrivning

Contrast media allergy

Datatyp

boolean

Alias
UMLS CUI [1]
C0570562
other primary malignancy
Beskrivning

Primary tumor Other

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0677930
UMLS CUI [1,2]
C0205394
acute viral hepatitis
Beskrivning

Viral hepatitis

Datatyp

boolean

Alias
UMLS CUI [1]
C0042721
prior history of liver transplantation
Beskrivning

Transplantation of liver

Datatyp

boolean

Alias
UMLS CUI [1]
C0023911
thrombosis in splenic vein or portal vein
Beskrivning

Splenic vein thrombosis | Portal vein thrombosis

Datatyp

boolean

Alias
UMLS CUI [1]
C0272416
UMLS CUI [2]
C0155773
patients who were enrolled to other clinical trials within 4 weeks
Beskrivning

Study Subject Participation Status | Clinical Trials

Datatyp

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2]
C0008976
other severe chronic disease or psychiatric disease
Beskrivning

Chronic disease Severe | Mental Disorder, Severe

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0008679
UMLS CUI [1,2]
C0205082
UMLS CUI [2]
C4046029
pregnant or milk-feeding women
Beskrivning

Pregnancy | Breast Feeding

Datatyp

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
patients with coagulopathy, high risk of bleeding for the liver biopsy
Beskrivning

Blood Coagulation Disorders | High risk of bleeding Biopsy of liver

Datatyp

boolean

Alias
UMLS CUI [1]
C0005779
UMLS CUI [2,1]
C4039184
UMLS CUI [2,2]
C0193388
patients who disagree to participate in this study
Beskrivning

Study Subject Participation Status Disagreement

Datatyp

boolean

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C0680238

Similar models

Eligibility Hepatic Fibrosis NCT01447667

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
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])
Liver carcinoma TNM clinical staging
Item
ajcc stage i hcc
boolean
C2239176 (UMLS CUI [1,1])
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])
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])
Item Group
C0680251 (UMLS CUI)
Decreased renal function | Glomerular Filtration Rate
Item
decreased kidney function (gfr < 70 ml/min/kg)
boolean
C0232807 (UMLS CUI [1])
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])
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])
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])
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])
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])
Pregnancy | Breast Feeding
Item
pregnant or milk-feeding women
boolean
C0032961 (UMLS CUI [1])
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])
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])

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