ID

34386

Beskrivning

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

Länk

https://clinicaltrials.gov/show/NCT01501240

Nyckelord

  1. 2019-01-17 2019-01-17 -
  2. 2019-05-14 2019-05-14 -
Rättsinnehavare

see on clinicaltrials.gov

Uppladdad den

17 januari 2019

DOI

För en begäran logga in.

Licens

Creative Commons BY-NC 3.0

Modellkommentarer :

Här kan du kommentera modellen. Med hjälp av pratbubblor i Item-grupperna och Item kan du lägga in specifika kommentarer.

Itemgroup-kommentar för :

Item-kommentar för :

Du måste vara inloggad för att kunna ladda ner formulär. Var vänlig logga in eller registrera dig utan kostnad.

Eligibility Liver Cirrhosis NCT01501240

Eligibility Liver Cirrhosis NCT01501240

Inclusion Criteria
Beskrivning

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
Beskrivning

ID.1

Datatyp

boolean

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

ID.2

Datatyp

boolean

Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients under 20 years of age
Beskrivning

ID.3

Datatyp

boolean

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

ID.4

Datatyp

boolean

patients who underwent transarterial chemotherapy or radiofrequency ablation
Beskrivning

ID.5

Datatyp

boolean

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

ID.6

Datatyp

boolean

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

ID.7

Datatyp

boolean

patients with a contraindication for mr
Beskrivning

ID.8

Datatyp

boolean

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

ID.9

Datatyp

boolean

Similar models

Eligibility Liver Cirrhosis NCT01501240

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
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

Använd detta formulär för feedback, frågor och förslag på förbättringar.

Fält markerade med * är obligatoriska.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial