ID

44348

Beschreibung

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

Stichworte

Versionen (2)
  1. 26.01.20 26.01.20 -
  2. 20.09.21 20.09.21 -
Rechteinhaber

See clinicaltrials.gov

Hochgeladen am

20. September 2021

DOI

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Lizenz

Creative Commons BY 4.0
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Eligibility Hepatic Fibrosis NCT01447667

Englisch

Eligibility Hepatic Fibrosis NCT01447667

1 Formulare  
Inclusion Criteria
Beschreibung

Inclusion Criteria

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

Liver carcinoma hypervascular single

Datentyp

boolean

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

Liver carcinoma TNM clinical staging

Datentyp

boolean

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

Child-Pugh Classification

Datentyp

boolean

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

Radiofrequency ablation Liver carcinoma Planned

Datentyp

boolean

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

Agreement Voluntary Clinical Trial

Datentyp

boolean

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

Exclusion Criteria

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

Decreased renal function | Glomerular Filtration Rate

Datentyp

boolean

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

Medical contraindication MRI | Pacemaker | Defibrillator

Datentyp

boolean

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

Contrast media allergy

Datentyp

boolean

Alias
UMLS CUI [1]
C0570562
other primary malignancy
Beschreibung

Primary tumor Other

Datentyp

boolean

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

Viral hepatitis

Datentyp

boolean

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

Transplantation of liver

Datentyp

boolean

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

Splenic vein thrombosis | Portal vein thrombosis

Datentyp

boolean

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

Study Subject Participation Status | Clinical Trials

Datentyp

boolean

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

Chronic disease Severe | Mental Disorder, Severe

Datentyp

boolean

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

Pregnancy | Breast Feeding

Datentyp

boolean

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

Blood Coagulation Disorders | High risk of bleeding Biopsy of liver

Datentyp

boolean

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

Study Subject Participation Status Disagreement

Datentyp

boolean

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C0680238
Zum Seitenanfang zurückkehren

Ähnliche Modelle

Eligibility Hepatic Fibrosis NCT01447667

1 Formulare
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
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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