ID

34386

Descrição

Gadoxetic Acid-enhanced MR Evaluation of Hepatocellular Carcinoma and Dysplastic Nodules in the Cirrhotic Liver; ODM derived from: https://clinicaltrials.gov/show/NCT01501240

Link

https://clinicaltrials.gov/show/NCT01501240

Palavras-chave

Versões (2)
  1. 17/01/2019 17/01/2019 -
  2. 14/05/2019 14/05/2019 -
Titular dos direitos

see on clinicaltrials.gov

Transferido a

17 de janeiro de 2019

DOI

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Licença

Creative Commons BY-NC 3.0
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Eligibility Liver Cirrhosis NCT01501240

Inglês

Eligibility Liver Cirrhosis NCT01501240

1 Formulários  
Inclusion Criteria
Descrição

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients with known liver cirrhosis based on either histology, or a combination of physical examination, laboratory tests, and imaging data
Descrição

ID.1

Tipo de dados

boolean

patients with known liver cirrhosis based on either histology, or a combination of physical examination, laboratory tests, and imaging data
Descrição

ID.2

Tipo de dados

boolean

Exclusion Criteria
Descrição

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients under 20 years of age
Descrição

ID.3

Tipo de dados

boolean

patients who have more than 10 nodules detected on hepatobiliary phase of gadoxetic acid-enhanced mr
Descrição

ID.4

Tipo de dados

boolean

patients who underwent transarterial chemotherapy or radiofrequency ablation
Descrição

ID.5

Tipo de dados

boolean

women who are pregnant, lactating or who are of childbearing potential
Descrição

ID.6

Tipo de dados

boolean

patients with any physical or mental status than interferes with the signing of informed consent
Descrição

ID.7

Tipo de dados

boolean

patients with a contraindication for mr
Descrição

ID.8

Tipo de dados

boolean

patients with impaired renal function (e.g. acute renal failure or egfr < 30 ml/min/1.73m2) or patients on dialysis
Descrição

ID.9

Tipo de dados

boolean

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Similar models

Eligibility Liver Cirrhosis NCT01501240

1 Formulários
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
patients with known liver cirrhosis based on either histology, or a combination of physical examination, laboratory tests, and imaging data
boolean
ID.2
Item
patients with known liver cirrhosis based on either histology, or a combination of physical examination, laboratory tests, and imaging data
boolean
Item Group
C0680251 (UMLS CUI)
ID.3
Item
patients under 20 years of age
boolean
ID.4
Item
patients who have more than 10 nodules detected on hepatobiliary phase of gadoxetic acid-enhanced mr
boolean
ID.5
Item
patients who underwent transarterial chemotherapy or radiofrequency ablation
boolean
ID.6
Item
women who are pregnant, lactating or who are of childbearing potential
boolean
ID.7
Item
patients with any physical or mental status than interferes with the signing of informed consent
boolean
ID.8
Item
patients with a contraindication for mr
boolean
ID.9
Item
patients with impaired renal function (e.g. acute renal failure or egfr < 30 ml/min/1.73m2) or patients on dialysis
boolean
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