ID
44238
Description
A Open Label Study to Assess the Long-term Safety, Tolerability and Efficacy of Ambrisentan in Subjects With Inoperable Chronic Thromboembolic Pulmonary Hypertension (CTEPH); ODM derived from: https://clinicaltrials.gov/show/NCT01894022
Link
https://clinicaltrials.gov/show/NCT01894022
Keywords
Versions (2)
- 4/15/19 4/15/19 -
- 9/20/21 9/20/21 -
Copyright Holder
See clinicaltrials.gov
Uploaded on
September 20, 2021
DOI
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License
Creative Commons BY 4.0
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Eligibility Hypertension NCT01894022
Eligibility Hypertension NCT01894022
- StudyEvent: Eligibility
Description
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Description
ambrisentan
Data type
boolean
Alias
- UMLS CUI [1]
- C1176329
Description
Hypersensitivity Investigational New Drugs | Hypersensitivity Metabolite | Hypersensitivity Formulation Excipient
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0020517
- UMLS CUI [1,2]
- C0013230
- UMLS CUI [2,1]
- C0020517
- UMLS CUI [2,2]
- C0870883
- UMLS CUI [3,1]
- C0020517
- UMLS CUI [3,2]
- C0524527
- UMLS CUI [3,3]
- C0015237
Description
Pregnancy | Breast Feeding | Gender Contraceptive methods Refused
Data type
boolean
Alias
- UMLS CUI [1]
- C0032961
- UMLS CUI [2]
- C0006147
- UMLS CUI [3,1]
- C0079399
- UMLS CUI [3,2]
- C0700589
- UMLS CUI [3,3]
- C1705116
Description
Alanine aminotransferase increased | Aspartate aminotransferase increased
Data type
boolean
Alias
- UMLS CUI [1]
- C0151905
- UMLS CUI [2]
- C0151904
Description
Elevated total bilirubin | Bilirubin, direct measurement
Data type
boolean
Alias
- UMLS CUI [1]
- C0741494
- UMLS CUI [2]
- C0201916
Description
Renal Insufficiency Severe | Estimation of creatinine clearance by Cockcroft-Gault formula
Data type
boolean
Alias
- UMLS CUI [1,1]
- C1565489
- UMLS CUI [1,2]
- C0205082
- UMLS CUI [2]
- C2711451
Description
Hepatic impairment Moderate Child-Pugh Classification | Hepatic impairment Severe Child-Pugh Classification | Liver Cirrhosis | Liver Cirrhosis Absent
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0948807
- UMLS CUI [1,2]
- C0205081
- UMLS CUI [1,3]
- C4050412
- UMLS CUI [2,1]
- C0948807
- UMLS CUI [2,2]
- C0205082
- UMLS CUI [2,3]
- C4050412
- UMLS CUI [3]
- C0023890
- UMLS CUI [4,1]
- C0023890
- UMLS CUI [4,2]
- C0332197
Description
Body fluid retention
Data type
boolean
Alias
- UMLS CUI [1]
- C0268000
Description
Anemia
Data type
boolean
Alias
- UMLS CUI [1]
- C0002871
Description
Study Subject Participation Status | Investigational New Drugs
Data type
boolean
Alias
- UMLS CUI [1]
- C2348568
- UMLS CUI [2]
- C0013230
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Eligibility Hypertension NCT01894022
- StudyEvent: Eligibility
C0013230 (UMLS CUI [2])
C3831118 (UMLS CUI [2,1])
C1533716 (UMLS CUI [2,2])
C0035647 (UMLS CUI [2,3])
C0232910 (UMLS CUI [2,4])
C3831118 (UMLS CUI [3,1])
C1533716 (UMLS CUI [3,2])
C0700589 (UMLS CUI [3,3])
C0079399 (UMLS CUI [4,1])
C1533716 (UMLS CUI [4,2])
C0035647 (UMLS CUI [4,3])
C0156312 (UMLS CUI [4,4])
C0079399 (UMLS CUI [5,1])
C1533716 (UMLS CUI [5,2])
C0035647 (UMLS CUI [5,3])
C1704202 (UMLS CUI [5,4])
C0013230 (UMLS CUI [1,2])
C1533716 (UMLS CUI [2,1])
C0949266 (UMLS CUI [2,2])
C1510826 (UMLS CUI [1,2])
C0037435 (UMLS CUI [2,1])
C1550502 (UMLS CUI [2,2])
C0013230 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C0870883 (UMLS CUI [2,2])
C0020517 (UMLS CUI [3,1])
C0524527 (UMLS CUI [3,2])
C0015237 (UMLS CUI [3,3])
C0006147 (UMLS CUI [2])
C0079399 (UMLS CUI [3,1])
C0700589 (UMLS CUI [3,2])
C1705116 (UMLS CUI [3,3])
C0151904 (UMLS CUI [2])
C0201916 (UMLS CUI [2])
C0205082 (UMLS CUI [1,2])
C2711451 (UMLS CUI [2])
C0205081 (UMLS CUI [1,2])
C4050412 (UMLS CUI [1,3])
C0948807 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
C4050412 (UMLS CUI [2,3])
C0023890 (UMLS CUI [3])
C0023890 (UMLS CUI [4,1])
C0332197 (UMLS CUI [4,2])
C0013230 (UMLS CUI [2])