ID
39202
Description
A Clinical Trial to Compare and Evaluate the Pharmacokinetic Characteristics and the Safety of Fimasartan in Hepatic Impairment Patients and Healthy Volunteers; ODM derived from: https://clinicaltrials.gov/show/NCT01146938
Link
https://clinicaltrials.gov/show/NCT01146938
Keywords
Versions (2)
- 12/10/19 12/10/19 -
- 9/20/21 9/20/21 -
Copyright Holder
See clinicaltrials.gov
Uploaded on
December 10, 2019
DOI
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License
Creative Commons BY 4.0
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Eligibility Essential Hypertension NCT01146938
Eligibility Essential Hypertension NCT01146938
- StudyEvent: Eligibility
Description
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Description
Patient Hepatic impairment
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0030705
- UMLS CUI [1,2]
- C0948807
Description
Surgical Portosystemic Shunt
Data type
boolean
Alias
- UMLS CUI [1]
- C0032720
Description
Child-Pugh Classification
Data type
boolean
Alias
- UMLS CUI [1]
- C2347612
Description
Creatinine clearance measurement
Data type
boolean
Alias
- UMLS CUI [1]
- C0373595
Description
Ascites
Data type
boolean
Alias
- UMLS CUI [1]
- C0003962
Description
Healthy Volunteers
Data type
boolean
Alias
- UMLS CUI [1]
- C1708335
Description
Aspartate aminotransferase increased | Alanine aminotransferase increased
Data type
boolean
Alias
- UMLS CUI [1]
- C0151904
- UMLS CUI [2]
- C0151905
Description
Elevated total bilirubin
Data type
boolean
Alias
- UMLS CUI [1]
- C0741494
Description
Drug screen positive | Alcohol consumption screening Positive
Data type
boolean
Alias
- UMLS CUI [1]
- C0743295
- UMLS CUI [2,1]
- C0420032
- UMLS CUI [2,2]
- C1514241
Similar models
Eligibility Essential Hypertension NCT01146938
- StudyEvent: Eligibility
C0948807 (UMLS CUI [1,2])
C0948807 (UMLS CUI [1,2])
C0151905 (UMLS CUI [2])
C0420032 (UMLS CUI [2,1])
C1514241 (UMLS CUI [2,2])