ID

29279

Beschrijving

Observational Study to Estimate the Rates of Outcomes in Patients Undergoing Percutaneous Coronary Intervention (PCI) With Drug Eluting Stent (DES) Implantation Who Take Statins; ODM derived from: https://clinicaltrials.gov/show/NCT01047176

Link

https://clinicaltrials.gov/show/NCT01047176

Trefwoorden

Versies (1)
  1. 15-03-18 15-03-18 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

15 maart 2018

DOI

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Licentie

Creative Commons BY 4.0
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Eligibility Dyslipidemia NCT01047176

Engels

Eligibility Dyslipidemia NCT01047176

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
stable angina with indication to pci
Beschrijving

Stable angina | Indication Percutaneous Coronary Intervention

Datatype

boolean

Alias
UMLS CUI [1]
C0340288
UMLS CUI [2,1]
C3146298
UMLS CUI [2,2]
C1532338
hospitalization to russian cardiological research center (ркнпк) for pci procedure with drug-eluting stents implantation
Beschrijving

Hospitalization Percutaneous Coronary Intervention | Drug-Eluting Stents Implantation

Datatype

boolean

Alias
UMLS CUI [1,1]
C0019993
UMLS CUI [1,2]
C1532338
UMLS CUI [2,1]
C1322815
UMLS CUI [2,2]
C0021107
statin therapy initiated for at least one month prior to pci
Beschrijving

Statin therapy Initiation

Datatype

boolean

Alias
UMLS CUI [1,1]
C1278454
UMLS CUI [1,2]
C1704686
written informed consent provided prior the start of participation in the study.
Beschrijving

Informed Consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
subjects who are unwilling or unable to provide informed consent.
Beschrijving

Informed Consent Unwilling | Informed Consent Unable

Datatype

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0558080
UMLS CUI [2,1]
C0021430
UMLS CUI [2,2]
C1299582
presence of acs during the current hospitalization
Beschrijving

Acute Coronary Syndrome

Datatype

boolean

Alias
UMLS CUI [1]
C0948089
severe chf (nyha iii/iv) or lvef<40 %
Beschrijving

Congestive heart failure Severe New York Heart Association Classification | Left ventricular ejection fraction

Datatype

boolean

Alias
UMLS CUI [1,1]
C0018802
UMLS CUI [1,2]
C0205082
UMLS CUI [1,3]
C1275491
UMLS CUI [2]
C0428772
stroke within 6 months before pci
Beschrijving

Cerebrovascular accident

Datatype

boolean

Alias
UMLS CUI [1]
C0038454
acute or chronic inflammatory disease
Beschrijving

Inflammatory disorder | Chronic inflammatory disorder

Datatype

boolean

Alias
UMLS CUI [1]
C1290884
UMLS CUI [2]
C1290886
anti-inflammatory medications intake, with the exception of aspirin
Beschrijving

Anti-Inflammatory Agents | Exception Aspirin

Datatype

boolean

Alias
UMLS CUI [1]
C0003209
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C0004057
severe liver or muscle disease
Beschrijving

Liver disease Severe | Myopathy Severe

Datatype

boolean

Alias
UMLS CUI [1,1]
C0023895
UMLS CUI [1,2]
C0205082
UMLS CUI [2,1]
C0026848
UMLS CUI [2,2]
C0205082
severe kidney disease / renal failure with creatinine > 3 mg/dl
Beschrijving

Kidney Disease Severe | Kidney Failure | Creatinine measurement, serum

Datatype

boolean

Alias
UMLS CUI [1,1]
C0022658
UMLS CUI [1,2]
C0205082
UMLS CUI [2]
C0035078
UMLS CUI [3]
C0201976
history of oncologic disease
Beschrijving

Disease Oncologic

Datatype

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C0205478
conceivable impossibility to come in touch with the patient or his family at 1-year after the intervention
Beschrijving

Patient unavailable

Datatype

boolean

Alias
UMLS CUI [1]
C1301818
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Similar models

Eligibility Dyslipidemia NCT01047176

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Stable angina | Indication Percutaneous Coronary Intervention
Item
stable angina with indication to pci
boolean
C0340288 (UMLS CUI [1])
C3146298 (UMLS CUI [2,1])
C1532338 (UMLS CUI [2,2])
Hospitalization Percutaneous Coronary Intervention | Drug-Eluting Stents Implantation
Item
hospitalization to russian cardiological research center (ркнпк) for pci procedure with drug-eluting stents implantation
boolean
C0019993 (UMLS CUI [1,1])
C1532338 (UMLS CUI [1,2])
C1322815 (UMLS CUI [2,1])
C0021107 (UMLS CUI [2,2])
Statin therapy Initiation
Item
statin therapy initiated for at least one month prior to pci
boolean
C1278454 (UMLS CUI [1,1])
C1704686 (UMLS CUI [1,2])
Informed Consent
Item
written informed consent provided prior the start of participation in the study.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Informed Consent Unwilling | Informed Consent Unable
Item
subjects who are unwilling or unable to provide informed consent.
boolean
C0021430 (UMLS CUI [1,1])
C0558080 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2,1])
C1299582 (UMLS CUI [2,2])
Acute Coronary Syndrome
Item
presence of acs during the current hospitalization
boolean
C0948089 (UMLS CUI [1])
Congestive heart failure Severe New York Heart Association Classification | Left ventricular ejection fraction
Item
severe chf (nyha iii/iv) or lvef<40 %
boolean
C0018802 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C1275491 (UMLS CUI [1,3])
C0428772 (UMLS CUI [2])
Cerebrovascular accident
Item
stroke within 6 months before pci
boolean
C0038454 (UMLS CUI [1])
Inflammatory disorder | Chronic inflammatory disorder
Item
acute or chronic inflammatory disease
boolean
C1290884 (UMLS CUI [1])
C1290886 (UMLS CUI [2])
Anti-Inflammatory Agents | Exception Aspirin
Item
anti-inflammatory medications intake, with the exception of aspirin
boolean
C0003209 (UMLS CUI [1])
C1705847 (UMLS CUI [2,1])
C0004057 (UMLS CUI [2,2])
Liver disease Severe | Myopathy Severe
Item
severe liver or muscle disease
boolean
C0023895 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0026848 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
Kidney Disease Severe | Kidney Failure | Creatinine measurement, serum
Item
severe kidney disease / renal failure with creatinine > 3 mg/dl
boolean
C0022658 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0035078 (UMLS CUI [2])
C0201976 (UMLS CUI [3])
Disease Oncologic
Item
history of oncologic disease
boolean
C0012634 (UMLS CUI [1,1])
C0205478 (UMLS CUI [1,2])
Patient unavailable
Item
conceivable impossibility to come in touch with the patient or his family at 1-year after the intervention
boolean
C1301818 (UMLS CUI [1])
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