ID
28602
Beschrijving
The Nordic Bifurcation Study III; ODM derived from: https://clinicaltrials.gov/show/NCT00914199
Link
https://clinicaltrials.gov/show/NCT00914199
Trefwoorden
Versies (1)
- 24-01-18 24-01-18 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
24 januari 2018
DOI
Voor een aanvraag inloggen.
Licentie
Creative Commons BY 4.0
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Eligibility Coronary Artery Disease NCT00914199
Eligibility Coronary Artery Disease NCT00914199
- StudyEvent: Eligibility
Beschrijving
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Beschrijving
Age
Datatype
boolean
Alias
- UMLS CUI [1]
- C0001779
Beschrijving
ST segment elevation myocardial infarction
Datatype
boolean
Alias
- UMLS CUI [1]
- C1536220
Beschrijving
Life Expectancy
Datatype
boolean
Alias
- UMLS CUI [1]
- C0023671
Beschrijving
Creatinine measurement, serum
Datatype
boolean
Alias
- UMLS CUI [1]
- C0201976
Beschrijving
Aspirin allergy | Hypersensitivity Clopidogrel | Hypersensitivity Ticlopidine
Datatype
boolean
Alias
- UMLS CUI [1]
- C0004058
- UMLS CUI [2,1]
- C0020517
- UMLS CUI [2,2]
- C0070166
- UMLS CUI [3,1]
- C0020517
- UMLS CUI [3,2]
- C0040207
Beschrijving
Hypersensitivity Sirolimus
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0020517
- UMLS CUI [1,2]
- C0072980
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Eligibility Coronary Artery Disease NCT00914199
- StudyEvent: Eligibility
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C1305171 (UMLS CUI [5,2])
C0500492 (UMLS CUI [1,2])
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C1305727 (UMLS CUI [2,2])
C0226032 (UMLS CUI [2,3])
C1542147 (UMLS CUI [1,2])
C1301886 (UMLS CUI [1,3])
C0456389 (UMLS CUI [1,4])
C1253959 (UMLS CUI [1,2])
C1301886 (UMLS CUI [1,3])
C0456389 (UMLS CUI [1,4])
C0020517 (UMLS CUI [2,1])
C0070166 (UMLS CUI [2,2])
C0020517 (UMLS CUI [3,1])
C0040207 (UMLS CUI [3,2])
C0072980 (UMLS CUI [1,2])