Informações:
Falhas:
ID
29279
Descrição
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
Palavras-chave
Versões (1)
- 15/03/2018 15/03/2018 -
Titular dos direitos
See clinicaltrials.gov
Transferido a
15 de março de 2018
DOI
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Licença
Creative Commons BY 4.0
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Eligibility Dyslipidemia NCT01047176
Eligibility Dyslipidemia NCT01047176
- StudyEvent: Eligibility
Similar models
Eligibility Dyslipidemia NCT01047176
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])