ID

35544

Beschrijving

Comparison Between P2Y12 Antagonist Monotherapy and Dual Antiplatelet Therapy After DES; ODM derived from: https://clinicaltrials.gov/show/NCT02079194

Link

https://clinicaltrials.gov/show/NCT02079194

Trefwoorden

Versies (1)
  1. 08-03-19 08-03-19 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

8 maart 2019

DOI

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Licentie

Creative Commons BY 4.0
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Eligibility Coronary Artery Disease NCT02079194

Engels

Eligibility Coronary Artery Disease NCT02079194

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
subject must be at least 20 years of age.
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
subject is able to verbally confirm understandings of risks, benefits and treatment alternatives and he/she or his/her legally authorized representative provides written informed consent prior to any study related procedure.
Beschrijving

Comprehension Study Protocol | Informed Consent | Informed Consent Patient Representative

Datatype

boolean

Alias
UMLS CUI [1,1]
C0162340
UMLS CUI [1,2]
C2348563
UMLS CUI [2]
C0021430
UMLS CUI [3,1]
C0021430
UMLS CUI [3,2]
C0030701
patients undergoing successful pci
Beschrijving

Percutaneous Coronary Intervention Successful

Datatype

boolean

Alias
UMLS CUI [1,1]
C1532338
UMLS CUI [1,2]
C1272703
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
hemodynamic instability or cardiogenic shock
Beschrijving

Hemodynamic instability | Shock, Cardiogenic

Datatype

boolean

Alias
UMLS CUI [1]
C0948268
UMLS CUI [2]
C0036980
active bleeding
Beschrijving

Hemorrhage

Datatype

boolean

Alias
UMLS CUI [1]
C0019080
known hypersensitivity or contraindication to study medications
Beschrijving

Hypersensitivity Investigational New Drugs | Medical contraindication Investigational New Drugs

Datatype

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0013230
UMLS CUI [2,1]
C1301624
UMLS CUI [2,2]
C0013230
female of childbearing potential, unless a recent pregnancy test is negative, who possibly plan to become pregnant any time after enrollment into this study
Beschrijving

Childbearing Potential | Planned Pregnancy Possible | Exception Pregnancy test negative

Datatype

boolean

Alias
UMLS CUI [1]
C3831118
UMLS CUI [2,1]
C0032992
UMLS CUI [2,2]
C0332149
UMLS CUI [3,1]
C1705847
UMLS CUI [3,2]
C0427780
non-cardiac co-morbid conditions are present with life expectancy <2 year or that may result in protocol non-compliance (per site investigator's medical judgment).
Beschrijving

Comorbidity | Exception Heart Diseases | Life Expectancy | Compliance behavior Lacking

Datatype

boolean

Alias
UMLS CUI [1]
C0009488
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C0018799
UMLS CUI [3]
C0023671
UMLS CUI [4,1]
C1321605
UMLS CUI [4,2]
C0332268
angiographic exclusion criteria
Beschrijving

Exclusion Criteria Angiography

Datatype

boolean

Alias
UMLS CUI [1,1]
C0680251
UMLS CUI [1,2]
C0002978
bifurcation lesions requiring side branch stenting
Beschrijving

Bifurcation lesion | Requirement Side Branch Stenting

Datatype

boolean

Alias
UMLS CUI [1]
C1299363
UMLS CUI [2,1]
C1514873
UMLS CUI [2,2]
C0441987
UMLS CUI [2,3]
C0500459
UMLS CUI [2,4]
C2348535
lesions treated with 3 or more overlapped stents
Beschrijving

Lesions | Stent overlapped Quantity

Datatype

boolean

Alias
UMLS CUI [1]
C0221198
UMLS CUI [2,1]
C0038257
UMLS CUI [2,2]
C0185027
UMLS CUI [2,3]
C1265611
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Similar models

Eligibility Coronary Artery Disease NCT02079194

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
subject must be at least 20 years of age.
boolean
C0001779 (UMLS CUI [1])
Comprehension Study Protocol | Informed Consent | Informed Consent Patient Representative
Item
subject is able to verbally confirm understandings of risks, benefits and treatment alternatives and he/she or his/her legally authorized representative provides written informed consent prior to any study related procedure.
boolean
C0162340 (UMLS CUI [1,1])
C2348563 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2])
C0021430 (UMLS CUI [3,1])
C0030701 (UMLS CUI [3,2])
Percutaneous Coronary Intervention Successful
Item
patients undergoing successful pci
boolean
C1532338 (UMLS CUI [1,1])
C1272703 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Hemodynamic instability | Shock, Cardiogenic
Item
hemodynamic instability or cardiogenic shock
boolean
C0948268 (UMLS CUI [1])
C0036980 (UMLS CUI [2])
Hemorrhage
Item
active bleeding
boolean
C0019080 (UMLS CUI [1])
Hypersensitivity Investigational New Drugs | Medical contraindication Investigational New Drugs
Item
known hypersensitivity or contraindication to study medications
boolean
C0020517 (UMLS CUI [1,1])
C0013230 (UMLS CUI [1,2])
C1301624 (UMLS CUI [2,1])
C0013230 (UMLS CUI [2,2])
Childbearing Potential | Planned Pregnancy Possible | Exception Pregnancy test negative
Item
female of childbearing potential, unless a recent pregnancy test is negative, who possibly plan to become pregnant any time after enrollment into this study
boolean
C3831118 (UMLS CUI [1])
C0032992 (UMLS CUI [2,1])
C0332149 (UMLS CUI [2,2])
C1705847 (UMLS CUI [3,1])
C0427780 (UMLS CUI [3,2])
Comorbidity | Exception Heart Diseases | Life Expectancy | Compliance behavior Lacking
Item
non-cardiac co-morbid conditions are present with life expectancy <2 year or that may result in protocol non-compliance (per site investigator's medical judgment).
boolean
C0009488 (UMLS CUI [1])
C1705847 (UMLS CUI [2,1])
C0018799 (UMLS CUI [2,2])
C0023671 (UMLS CUI [3])
C1321605 (UMLS CUI [4,1])
C0332268 (UMLS CUI [4,2])
Exclusion Criteria Angiography
Item
angiographic exclusion criteria
boolean
C0680251 (UMLS CUI [1,1])
C0002978 (UMLS CUI [1,2])
Bifurcation lesion | Requirement Side Branch Stenting
Item
bifurcation lesions requiring side branch stenting
boolean
C1299363 (UMLS CUI [1])
C1514873 (UMLS CUI [2,1])
C0441987 (UMLS CUI [2,2])
C0500459 (UMLS CUI [2,3])
C2348535 (UMLS CUI [2,4])
Lesions | Stent overlapped Quantity
Item
lesions treated with 3 or more overlapped stents
boolean
C0221198 (UMLS CUI [1])
C0038257 (UMLS CUI [2,1])
C0185027 (UMLS CUI [2,2])
C1265611 (UMLS CUI [2,3])
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