ID

33857

Beschrijving

The Real-world Firebird 2 Versus Cypher Sirolimus-eluting Stent in Treating Patients With Coronary Artery Disease; ODM derived from: https://clinicaltrials.gov/show/NCT01328730

Link

https://clinicaltrials.gov/show/NCT01328730

Trefwoorden

Versies (1)
  1. 04-01-19 04-01-19 -
Houder van rechten

Shanghai Jiao Tong University School of Medicine

Geüploaded op

4 januari 2019

DOI

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Licentie

Creative Commons BY-NC 3.0
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Eligibility Coronary Artery Stenosis NCT01328730

Engels

Eligibility Coronary Artery Stenosis NCT01328730

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
Age > 18 years
Beschrijving

Age of patient

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
Patient is male or un-pregnant female
Beschrijving

Gender of Patient, pregnancy

Datatype

boolean

Alias
UMLS CUI [1,1]
C0079399
UMLS CUI [1,2]
C0032961
UMLS CUI [1,3]
C0332197
Stenosis > 70% in one of the major epicardial coronary arteries
Beschrijving

Stenosis > 70% in one of the major epicardial coronary arteries

Datatype

boolean

Alias
UMLS CUI [1,1]
C0242231
UMLS CUI [1,2]
C0442016
UMLS CUI [1,3]
C0205164
No contra-indications of stent implantation existing
Beschrijving

No contra-indications of stent implantation existing

Datatype

boolean

Alias
UMLS CUI [1,1]
C0521232
UMLS CUI [1,2]
C1301624
UMLS CUI [1,3]
C0332197
Patient signed the informed consent
Beschrijving

Patient signed the informed consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
Did the Patient suffer from acute myocardial infarction within one week?
Beschrijving

Acute myocardial infarction within one week

Datatype

boolean

Alias
UMLS CUI [1]
C0155626
Patient has contra-indications of stent implantation or can not tolerate dual antiplatelet therapy
Beschrijving

Patient has contra-indications of stent implantation or can not tolerate dual antiplatelet therapy

Datatype

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0521232
UMLS CUI [2,1]
C0277585
UMLS CUI [2,2]
C1096021
UMLS CUI [2,3]
C1554184
No history of stent implantation within last one-year
Beschrijving

No history of stent implantation within last one-year

Datatype

boolean

Alias
UMLS CUI [1,1]
C0521232
UMLS CUI [1,2]
C0262926
UMLS CUI [1,3]
C0332197
Patient received other brand coronary stent during index procedure
Beschrijving

Patient received other brand coronary stent during index procedure

Datatype

boolean

Alias
UMLS CUI [1,1]
C0592503
UMLS CUI [1,2]
C0687568
No achievement of informed consent
Beschrijving

No Achievement of informed consent

Datatype

boolean

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

Eligibility Coronary Artery Stenosis NCT01328730

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
Age > 18 years
boolean
C0001779 (UMLS CUI [1])
Gender
Item
Patient is male or un-pregnant female
boolean
C0079399 (UMLS CUI [1,1])
C0032961 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
Coronary stenosis
Item
Stenosis > 70% in one of the major epicardial coronary arteries
boolean
C0242231 (UMLS CUI [1,1])
C0442016 (UMLS CUI [1,2])
C0205164 (UMLS CUI [1,3])
Contra-indications of stent implantation
Item
No contra-indications of stent implantation existing
boolean
C0521232 (UMLS CUI [1,1])
C1301624 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
Signed informed consent
Item
Patient signed the informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Acute myocardial infarction
Item
Did the Patient suffer from acute myocardial infarction within one week?
boolean
C0155626 (UMLS CUI [1])
Contra-indications of stent implantation or intolerance to dual antiplatlet therapy
Item
Patient has contra-indications of stent implantation or can not tolerate dual antiplatelet therapy
boolean
C1301624 (UMLS CUI [1,1])
C0521232 (UMLS CUI [1,2])
C0277585 (UMLS CUI [2,1])
C1096021 (UMLS CUI [2,2])
C1554184 (UMLS CUI [2,3])
History of stent implantation
Item
No history of stent implantation within last one-year
boolean
C0521232 (UMLS CUI [1,1])
C0262926 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
Other brand coronary stent
Item
Patient received other brand coronary stent during index procedure
boolean
C0592503 (UMLS CUI [1,1])
C0687568 (UMLS CUI [1,2])
Achievement of informed consent
Item
No achievement of informed consent
boolean
C0021430 (UMLS CUI [1,1])
C0332268 (UMLS CUI [1,2])
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