Information:
Error:
ID
33601
Description
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
Keywords
Versions (1)
- 12/15/18 12/15/18 -
Copyright Holder
See clinicaltrials.gov
Uploaded on
December 15, 2018
DOI
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License
Creative Commons BY 4.0
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Eligibility Coronary Artery Disease NCT01373632
Eligibility Coronary Artery Disease NCT01373632
- StudyEvent: Eligibility
Similar models
Eligibility Coronary Artery Disease NCT01373632
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
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])
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])
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])
C0332197 (UMLS CUI [1,2])
C0522776 (UMLS CUI [1,3])
Informed Consent
Item
singed the informed consent
boolean
C0021430 (UMLS CUI [1])
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])
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])
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])
C0332268 (UMLS CUI [1,2])