ID
36446
Descripción
Gadoxetic Acid-enhanced MR Evaluation of Hepatocellular Carcinoma and Dysplastic Nodules in the Cirrhotic Liver; ODM derived from: https://clinicaltrials.gov/show/NCT01501240 Brief Summary: A prospective intra-individual study to investigate the diagnostic performance of gadoxetic acid-enhanced MR for the patients with liver cirrhosis using thin-section whole-explant as standard of reference
Link
https://clinicaltrials.gov/show/NCT01501240
Palabras clave
Versiones (2)
- 17/1/19 17/1/19 -
- 14/5/19 14/5/19 -
Titular de derechos de autor
Jae Ho Byun
Subido en
14 de mayo de 2019
DOI
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Licencia
Creative Commons BY-NC 3.0
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MR Evaluation of Hepatocellular Carcinoma NCT01501240
Eligibility Criteria
- StudyEvent: Eligibility
Descripción
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Descripción
Age
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0001779
Descripción
Patients under 20 years of age (are to be excluded)
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0745761
- UMLS CUI [1,2]
- C0449788
- UMLS CUI [1,3]
- C3496055
- UMLS CUI [1,4]
- C3489483
- UMLS CUI [1,5]
- C0024485
Descripción
Assess if the patient was treated with chemo or radiotherapy
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0522522
- UMLS CUI [1,2]
- C3665472
- UMLS CUI [2]
- C0850292
Descripción
women who are pregnant, lactating or who are of childbearing potential (are to be excluded)
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0032961
- UMLS CUI [2]
- C3831118
- UMLS CUI [3]
- C0022925
Descripción
patients with any physical or mental status that interferes with the signing of informed consent (are to be excluded)
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0597240
- UMLS CUI [1,2]
- C0521102
- UMLS CUI [1,3]
- C1519316
- UMLS CUI [1,4]
- C0021430
- UMLS CUI [2,1]
- C0278060
- UMLS CUI [2,2]
- C0521102
- UMLS CUI [2,3]
- C1519316
- UMLS CUI [2,4]
- C0021430
Descripción
patients with a contraindication for mr (are to be excluded)
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0024485
- UMLS CUI [1,2]
- C1301624
Descripción
patients with impaired renal function (e.g. acute renal failure or egfr < 30 ml/min/1.73m2) or patients on dialysis (are to be excluded)
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0232804
- UMLS CUI [1,2]
- C0221099
- UMLS CUI [2]
- C0011946
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Eligibility Criteria
- StudyEvent: Eligibility
C0019638 (UMLS CUI [1,2])
C0023890 (UMLS CUI [2,1])
C0205195 (UMLS CUI [2,2])
C0031809 (UMLS CUI [2,3])
C0022885 (UMLS CUI [2,4])
C0025086 (UMLS CUI [2,5])
C0449788 (UMLS CUI [1,2])
C3496055 (UMLS CUI [1,3])
C3489483 (UMLS CUI [1,4])
C0024485 (UMLS CUI [1,5])
C3665472 (UMLS CUI [1,2])
C0850292 (UMLS CUI [2])
C3831118 (UMLS CUI [2])
C0022925 (UMLS CUI [3])
C0521102 (UMLS CUI [1,2])
C1519316 (UMLS CUI [1,3])
C0021430 (UMLS CUI [1,4])
C0278060 (UMLS CUI [2,1])
C0521102 (UMLS CUI [2,2])
C1519316 (UMLS CUI [2,3])
C0021430 (UMLS CUI [2,4])
C1301624 (UMLS CUI [1,2])
C0221099 (UMLS CUI [1,2])
C0011946 (UMLS CUI [2])