ID
44238
Beschrijving
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
Trefwoorden
Versies (2)
- 15-04-19 15-04-19 -
- 20-09-21 20-09-21 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
20 september 2021
DOI
Voor een aanvraag inloggen.
Licentie
Creative Commons BY 4.0
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Eligibility Hypertension NCT01894022
Eligibility Hypertension NCT01894022
- StudyEvent: Eligibility
Beschrijving
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Beschrijving
ambrisentan
Datatype
boolean
Alias
- UMLS CUI [1]
- C1176329
Beschrijving
Hypersensitivity Investigational New Drugs | Hypersensitivity Metabolite | Hypersensitivity Formulation Excipient
Datatype
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
Beschrijving
Pregnancy | Breast Feeding | Gender Contraceptive methods Refused
Datatype
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
Beschrijving
Alanine aminotransferase increased | Aspartate aminotransferase increased
Datatype
boolean
Alias
- UMLS CUI [1]
- C0151905
- UMLS CUI [2]
- C0151904
Beschrijving
Elevated total bilirubin | Bilirubin, direct measurement
Datatype
boolean
Alias
- UMLS CUI [1]
- C0741494
- UMLS CUI [2]
- C0201916
Beschrijving
Renal Insufficiency Severe | Estimation of creatinine clearance by Cockcroft-Gault formula
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1565489
- UMLS CUI [1,2]
- C0205082
- UMLS CUI [2]
- C2711451
Beschrijving
Hepatic impairment Moderate Child-Pugh Classification | Hepatic impairment Severe Child-Pugh Classification | Liver Cirrhosis | Liver Cirrhosis Absent
Datatype
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
Beschrijving
Body fluid retention
Datatype
boolean
Alias
- UMLS CUI [1]
- C0268000
Beschrijving
Anemia
Datatype
boolean
Alias
- UMLS CUI [1]
- C0002871
Beschrijving
Study Subject Participation Status | Investigational New Drugs
Datatype
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])