ID
40824
Beschrijving
Primary Prevention of Major Adverse Cardiac Events (MACE) With Standard and Intensive Statin Treatment in Patients With Diabetes: Survival and Cardiovascular Event Assessments; ODM derived from: https://clinicaltrials.gov/show/NCT01173939
Link
https://clinicaltrials.gov/show/NCT01173939
Trefwoorden
Versies (1)
- 19-05-20 19-05-20 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
19 mei 2020
DOI
Voor een aanvraag inloggen.
Licentie
Creative Commons BY 4.0
Model Commentaren :
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Eligibility Hypercholesterolemia NCT01173939
Eligibility Hypercholesterolemia NCT01173939
- StudyEvent: Eligibility
Beschrijving
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Beschrijving
Exclusion Criteria Fulfill
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0680251
- UMLS CUI [1,2]
- C1550543
Beschrijving
rosuvastatin | pitavastatin | atorvastatin
Datatype
boolean
Alias
- UMLS CUI [1]
- C0965129
- UMLS CUI [2]
- C1101838
- UMLS CUI [3]
- C0286651
Beschrijving
Hypercholesterolemia, Familial
Datatype
boolean
Alias
- UMLS CUI [1]
- C0020445
Beschrijving
Serum Triglyceride Measurement
Datatype
boolean
Alias
- UMLS CUI [1]
- C0542495
Beschrijving
Myocardial Infarction
Datatype
boolean
Alias
- UMLS CUI [1]
- C0027051
Beschrijving
Coronary revascularisation | Percutaneous Coronary Intervention | Coronary Artery Bypass Surgery
Datatype
boolean
Alias
- UMLS CUI [1]
- C0877341
- UMLS CUI [2]
- C1532338
- UMLS CUI [3]
- C0010055
Beschrijving
Therapy Unstable Angina
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0087111
- UMLS CUI [1,2]
- C0002965
Beschrijving
Cerebrovascular accident | Lacunar Infarction Asymptomatic Excluded
Datatype
boolean
Alias
- UMLS CUI [1]
- C0038454
- UMLS CUI [2,1]
- C0333559
- UMLS CUI [2,2]
- C0231221
- UMLS CUI [2,3]
- C0332196
Beschrijving
Heart failure
Datatype
boolean
Alias
- UMLS CUI [1]
- C0018801
Beschrijving
Statin allergy
Datatype
boolean
Alias
- UMLS CUI [1]
- C0571873
Beschrijving
Drug-induced myopathy
Datatype
boolean
Alias
- UMLS CUI [1]
- C0410220
Beschrijving
Cardiac Arrhythmia Poorly controlled
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0003811
- UMLS CUI [1,2]
- C3853134
Beschrijving
Liver disease Severe | Kidney Disease Severe
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0023895
- UMLS CUI [1,2]
- C0205082
- UMLS CUI [2,1]
- C0022658
- UMLS CUI [2,2]
- C0205082
Beschrijving
Comorbidity Serious | Malignant Neoplasm | Lifespan Limited Severely
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0009488
- UMLS CUI [1,2]
- C0205404
- UMLS CUI [2]
- C0006826
- UMLS CUI [3,1]
- C0870809
- UMLS CUI [3,2]
- C0439801
- UMLS CUI [3,3]
- C0205082
Beschrijving
Pregnancy | Possible pregnancy
Datatype
boolean
Alias
- UMLS CUI [1]
- C0032961
- UMLS CUI [2]
- C0425965
Beschrijving
Study Subject Participation Status Ineligible
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C2348568
- UMLS CUI [1,2]
- C1512714
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Eligibility Hypercholesterolemia NCT01173939
- StudyEvent: Eligibility
C1550543 (UMLS CUI [1,2])
C0428474 (UMLS CUI [2])
C0030705 (UMLS CUI [3,1])
C0332155 (UMLS CUI [3,2])
C0030705 (UMLS CUI [4,1])
C1522326 (UMLS CUI [4,2])
C0474680 (UMLS CUI [2])
C0013216 (UMLS CUI [3])
C0013216 (UMLS CUI [4,1])
C0332197 (UMLS CUI [4,2])
C0871470 (UMLS CUI [2])
C0428883 (UMLS CUI [3])
C0013216 (UMLS CUI [4])
C0013216 (UMLS CUI [5,1])
C0332197 (UMLS CUI [5,2])
C1265611 (UMLS CUI [1,2])
C0474680 (UMLS CUI [2])
C0205164 (UMLS CUI [1,2])
C0018787 (UMLS CUI [1,3])
C0241889 (UMLS CUI [2,1])
C0444502 (UMLS CUI [2,2])
C0241889 (UMLS CUI [3,1])
C0443298 (UMLS CUI [3,2])
C0033687 (UMLS CUI [2])
C3811844 (UMLS CUI [3])
C1550543 (UMLS CUI [1,2])
C1101838 (UMLS CUI [2])
C0286651 (UMLS CUI [3])
C1532338 (UMLS CUI [2])
C0010055 (UMLS CUI [3])
C0002965 (UMLS CUI [1,2])
C0333559 (UMLS CUI [2,1])
C0231221 (UMLS CUI [2,2])
C0332196 (UMLS CUI [2,3])
C3853134 (UMLS CUI [1,2])
C0205082 (UMLS CUI [1,2])
C0022658 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
C0205404 (UMLS CUI [1,2])
C0006826 (UMLS CUI [2])
C0870809 (UMLS CUI [3,1])
C0439801 (UMLS CUI [3,2])
C0205082 (UMLS CUI [3,3])
C0425965 (UMLS CUI [2])
C1512714 (UMLS CUI [1,2])