ID

29279

Beschreibung

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

Stichworte

Versionen (1)
  1. 15.03.18 15.03.18 -
Rechteinhaber

See clinicaltrials.gov

Hochgeladen am

15. März 2018

DOI

Für eine Beantragung loggen Sie sich ein.

Lizenz

Creative Commons BY 4.0
Modell Kommentare :

Hier können Sie das Modell kommentieren. Über die Sprechblasen an den Itemgruppen und Items können Sie diese spezifisch kommentieren.

Zurück zu Modell Kommentaren
Itemgroup Kommentare für :

Item Kommentare für :

Um Formulare herunterzuladen müssen Sie angemeldet sein. Bitte loggen Sie sich ein oder registrieren Sie sich kostenlos.

Eligibility Dyslipidemia NCT01047176

Englisch

Eligibility Dyslipidemia NCT01047176

1 Formulare  
Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
stable angina with indication to pci
Beschreibung

Stable angina | Indication Percutaneous Coronary Intervention

Datentyp

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
Beschreibung

Hospitalization Percutaneous Coronary Intervention | Drug-Eluting Stents Implantation

Datentyp

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
Beschreibung

Statin therapy Initiation

Datentyp

boolean

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

Informed Consent

Datentyp

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschreibung

Exclusion Criteria

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

Informed Consent Unwilling | Informed Consent Unable

Datentyp

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
Beschreibung

Acute Coronary Syndrome

Datentyp

boolean

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

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

Datentyp

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
Beschreibung

Cerebrovascular accident

Datentyp

boolean

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

Inflammatory disorder | Chronic inflammatory disorder

Datentyp

boolean

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

Anti-Inflammatory Agents | Exception Aspirin

Datentyp

boolean

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

Liver disease Severe | Myopathy Severe

Datentyp

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
Beschreibung

Kidney Disease Severe | Kidney Failure | Creatinine measurement, serum

Datentyp

boolean

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

Disease Oncologic

Datentyp

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
Beschreibung

Patient unavailable

Datentyp

boolean

Alias
UMLS CUI [1]
C1301818
Zum Seitenanfang zurückkehren

Ähnliche Modelle

Eligibility Dyslipidemia NCT01047176

1 Formulare
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
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])
Zum Seitenanfang zurückkehren 

Kontakt

Benutzen Sie dieses Formular für Rückmeldungen, Fragen und Verbesserungsvorschläge.

Mit * gekennzeichnete Felder sind notwendig.

Hilfe

Benötigen Sie Hilfe bei der Suche? Um mehr Details zu erfahren und die Suche effektiver nutzen zu können schauen Sie sich doch das entsprechende Video auf unserer Tutorial Seite an.

Zum Video