ID
40859
Beschrijving
Long-term Ambrisentan Extension Study for Pediatric Patients Who Participated in AMB112529; ODM derived from: https://clinicaltrials.gov/show/NCT01342952
Link
https://clinicaltrials.gov/show/NCT01342952
Trefwoorden
Versies (1)
- 26-05-20 26-05-20 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
26 mei 2020
DOI
Voor een aanvraag inloggen.
Licentie
Creative Commons BY 4.0
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Eligibility Hypertension, Pulmonary NCT01342952
Eligibility Hypertension, Pulmonary NCT01342952
- StudyEvent: Eligibility
Beschrijving
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Beschrijving
Ambrisentan Withdrawn Clinical Trial Specified
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1176329
- UMLS CUI [1,2]
- C1707825
- UMLS CUI [1,3]
- C0008976
- UMLS CUI [1,4]
- C0205369
Beschrijving
Protocol Compliance Lacking Clinical Trial Specified
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0525058
- UMLS CUI [1,2]
- C0332268
- UMLS CUI [1,3]
- C0008976
- UMLS CUI [1,4]
- C0205369
Beschrijving
Pregnancy | Breast Feeding
Datatype
boolean
Alias
- UMLS CUI [1]
- C0032961
- UMLS CUI [2]
- C0006147
Beschrijving
Renal Insufficiency Severe | Estimated creatine clearance
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1565489
- UMLS CUI [1,2]
- C0205082
- UMLS CUI [2]
- C1273051
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 | Clinical Trial | Investigational New Drugs
Datatype
boolean
Alias
- UMLS CUI [1]
- C2348568
- UMLS CUI [2]
- C0008976
- UMLS CUI [3]
- C0013230
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Eligibility Hypertension, Pulmonary NCT01342952
- StudyEvent: Eligibility
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C0205197 (UMLS CUI [1,2])
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C0205412 (UMLS CUI [2,2])
C0332271 (UMLS CUI [3,1])
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C1514873 (UMLS CUI [1,2])
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C2973725 (UMLS CUI [2,2])
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C2348568 (UMLS CUI [2,1])
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C0332197 (UMLS CUI [2,3])
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C0332268 (UMLS CUI [1,2])
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C1273051 (UMLS CUI [2])
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