ID

33601

Beschreibung

Firebird 2 Versus Excel Sirolimus-eluting Stent in Treating Real-world Patients With Coronary Artery Disease; ODM derived from: https://clinicaltrials.gov/show/NCT01373632

Link

https://clinicaltrials.gov/show/NCT01373632

Stichworte

  1. 15.12.18 15.12.18 -
Rechteinhaber

See clinicaltrials.gov

Hochgeladen am

15. Dezember 2018

DOI

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Lizenz

Creative Commons BY 4.0

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Eligibility Coronary Artery Disease NCT01373632

Eligibility Coronary Artery Disease NCT01373632

Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
age > 18 years
Beschreibung

Age

Datentyp

boolean

Alias
UMLS CUI [1]
C0001779
male or un-pregnant female
Beschreibung

Gender | Pregnancy Absent

Datentyp

boolean

Alias
UMLS CUI [1]
C0079399
UMLS CUI [2,1]
C0032961
UMLS CUI [2,2]
C0332197
stenosis > 70% in one of major the epicardial coronary arteries
Beschreibung

Stenosis Percentage | Coronary artery Epicardial Major Quantity

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1261287
UMLS CUI [1,2]
C0439165
UMLS CUI [2,1]
C0205042
UMLS CUI [2,2]
C0442016
UMLS CUI [2,3]
C0205164
UMLS CUI [2,4]
C1265611
no contra-indications of stent implantation
Beschreibung

Medical contraindication Absent Placement of stent

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0332197
UMLS CUI [1,3]
C0522776
singed the informed consent
Beschreibung

Informed Consent

Datentyp

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
acute myocardial infarction within one week
Beschreibung

Myocardial Infarction

Datentyp

boolean

Alias
UMLS CUI [1]
C0027051
have contra-indications of stent implantation or can not tolerate dual antiplatelet therapy
Beschreibung

Medical contraindication Placement of stent | Antiplatelet therapy Dual Unable

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0522776
UMLS CUI [2,1]
C1096021
UMLS CUI [2,2]
C0205173
UMLS CUI [2,3]
C1299582
no history of stent implantation within last one-year
Beschreibung

Previous stent placement

Datentyp

boolean

Alias
UMLS CUI [1]
C2114504
received other brand coronary stent during index procedure
Beschreibung

Brand Coronary stent

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0592503
UMLS CUI [1,2]
C0687568
with no achievement of informed consent
Beschreibung

Informed Consent Lacking

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0332268

Ähnliche Modelle

Eligibility Coronary Artery Disease NCT01373632

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
age > 18 years
boolean
C0001779 (UMLS CUI [1])
Gender | Pregnancy Absent
Item
male or un-pregnant female
boolean
C0079399 (UMLS CUI [1])
C0032961 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
Stenosis Percentage | Coronary artery Epicardial Major Quantity
Item
stenosis > 70% in one of major the epicardial coronary arteries
boolean
C1261287 (UMLS CUI [1,1])
C0439165 (UMLS CUI [1,2])
C0205042 (UMLS CUI [2,1])
C0442016 (UMLS CUI [2,2])
C0205164 (UMLS CUI [2,3])
C1265611 (UMLS CUI [2,4])
Medical contraindication Absent Placement of stent
Item
no contra-indications of stent implantation
boolean
C1301624 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0522776 (UMLS CUI [1,3])
Informed Consent
Item
singed the informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Myocardial Infarction
Item
acute myocardial infarction within one week
boolean
C0027051 (UMLS CUI [1])
Medical contraindication Placement of stent | Antiplatelet therapy Dual Unable
Item
have contra-indications of stent implantation or can not tolerate dual antiplatelet therapy
boolean
C1301624 (UMLS CUI [1,1])
C0522776 (UMLS CUI [1,2])
C1096021 (UMLS CUI [2,1])
C0205173 (UMLS CUI [2,2])
C1299582 (UMLS CUI [2,3])
Previous stent placement
Item
no history of stent implantation within last one-year
boolean
C2114504 (UMLS CUI [1])
Brand Coronary stent
Item
received other brand coronary stent during index procedure
boolean
C0592503 (UMLS CUI [1,1])
C0687568 (UMLS CUI [1,2])
Informed Consent Lacking
Item
with no achievement of informed consent
boolean
C0021430 (UMLS CUI [1,1])
C0332268 (UMLS CUI [1,2])

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