ID

28745

Description

Xience or Vision Stent Management of Angina in the Elderly; ODM derived from: https://clinicaltrials.gov/show/NCT02198716

Lien

https://clinicaltrials.gov/show/NCT02198716

Mots-clés

Versions (1)
  1. 31/01/2018 31/01/2018 -
Détendeur de droits

See clinicaltrials.gov

Téléchargé le

31 janvier 2018

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0
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Eligibility Coronary Artery Disease NCT02198716

Anglais

Eligibility Coronary Artery Disease NCT02198716

1 Formulaires  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
age>80
Description

Age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
stable angina or acute coronary syndrome
Description

Stable angina | Acute Coronary Syndrome

Type de données

boolean

Alias
UMLS CUI [1]
C0340288
UMLS CUI [2]
C0948089
coronary narrowing suitable for stenting that is either ≥15mm long and/or ≤3mm diameter.
Description

Coronary Stenosis Suitable Stenting | Coronary Stenosis Length | Coronary Stenosis Diameter Size

Type de données

boolean

Alias
UMLS CUI [1,1]
C0242231
UMLS CUI [1,2]
C3900053
UMLS CUI [1,3]
C2348535
UMLS CUI [2,1]
C0242231
UMLS CUI [2,2]
C1444754
UMLS CUI [3,1]
C0242231
UMLS CUI [3,2]
C1301886
UMLS CUI [3,3]
C0456389
any lesion with high risk of restenosis eg chronic total occlusion, bifurcation, severe calcification
Description

Lesion High risk of Restenosis | Chronic Total Occlusion | Bifurcation lesion | Calcification Severe

Type de données

boolean

Alias
UMLS CUI [1,1]
C0221198
UMLS CUI [1,2]
C0332167
UMLS CUI [1,3]
C0333186
UMLS CUI [2]
C3275069
UMLS CUI [3]
C1299363
UMLS CUI [4,1]
C0175895
UMLS CUI [4,2]
C0205082
any left main stem lesion
Description

Lesion Left coronary artery main stem

Type de données

boolean

Alias
UMLS CUI [1,1]
C0221198
UMLS CUI [1,2]
C0226031
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
acute st segment elevation myocardial infarction
Description

ST segment elevation myocardial infarction

Type de données

boolean

Alias
UMLS CUI [1]
C1536220
cardiogenic shock
Description

Shock, Cardiogenic

Type de données

boolean

Alias
UMLS CUI [1]
C0036980
platelet count =50 x 109/mm3
Description

Platelet Count measurement

Type de données

boolean

Alias
UMLS CUI [1]
C0032181
patient life expectancy < 1 year
Description

Life Expectancy

Type de données

boolean

Alias
UMLS CUI [1]
C0023671
known allergies to clopidogrel, aspirin, heparin, stainless steel, iv contrast or stent drug elutant
Description

Hypersensitivity clopidogrel | Aspirin allergy | Heparin allergy | Hypersensitivity Stainless Steel | Allergy to intravenous contrast media | Hypersensitivity Drug-Eluting Stents

Type de données

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0070166
UMLS CUI [2]
C0004058
UMLS CUI [3]
C0571776
UMLS CUI [4,1]
C0020517
UMLS CUI [4,2]
C0038126
UMLS CUI [5]
C2242530
UMLS CUI [6,1]
C0020517
UMLS CUI [6,2]
C1322815
recent major gi haemorrhage (within 3 months)
Description

Gastrointestinal Hemorrhage Major

Type de données

boolean

Alias
UMLS CUI [1,1]
C0017181
UMLS CUI [1,2]
C0205164
any previous cerebral bleeding episode
Description

Cerebral Hemorrhage Episode

Type de données

boolean

Alias
UMLS CUI [1,1]
C2937358
UMLS CUI [1,2]
C0332189
participation in another investigational drug or device study
Description

Study Subject Participation Status | Investigational New Drugs | Investigational Medical Device

Type de données

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2]
C0013230
UMLS CUI [3]
C2346570
patient unable to give consent
Description

Informed Consent Unable

Type de données

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1299582
clinical decision precluding the use of drug eluting stent
Description

Clinical decision Excludes Drug-Eluting Stent

Type de données

boolean

Alias
UMLS CUI [1,1]
C3845884
UMLS CUI [1,2]
C0332196
UMLS CUI [1,3]
C1322815
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Similar models

Eligibility Coronary Artery Disease NCT02198716

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
age>80
boolean
C0001779 (UMLS CUI [1])
Stable angina | Acute Coronary Syndrome
Item
stable angina or acute coronary syndrome
boolean
C0340288 (UMLS CUI [1])
C0948089 (UMLS CUI [2])
Coronary Stenosis Suitable Stenting | Coronary Stenosis Length | Coronary Stenosis Diameter Size
Item
coronary narrowing suitable for stenting that is either ≥15mm long and/or ≤3mm diameter.
boolean
C0242231 (UMLS CUI [1,1])
C3900053 (UMLS CUI [1,2])
C2348535 (UMLS CUI [1,3])
C0242231 (UMLS CUI [2,1])
C1444754 (UMLS CUI [2,2])
C0242231 (UMLS CUI [3,1])
C1301886 (UMLS CUI [3,2])
C0456389 (UMLS CUI [3,3])
Lesion High risk of Restenosis | Chronic Total Occlusion | Bifurcation lesion | Calcification Severe
Item
any lesion with high risk of restenosis eg chronic total occlusion, bifurcation, severe calcification
boolean
C0221198 (UMLS CUI [1,1])
C0332167 (UMLS CUI [1,2])
C0333186 (UMLS CUI [1,3])
C3275069 (UMLS CUI [2])
C1299363 (UMLS CUI [3])
C0175895 (UMLS CUI [4,1])
C0205082 (UMLS CUI [4,2])
Lesion Left coronary artery main stem
Item
any left main stem lesion
boolean
C0221198 (UMLS CUI [1,1])
C0226031 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
ST segment elevation myocardial infarction
Item
acute st segment elevation myocardial infarction
boolean
C1536220 (UMLS CUI [1])
Shock, Cardiogenic
Item
cardiogenic shock
boolean
C0036980 (UMLS CUI [1])
Platelet Count measurement
Item
platelet count =50 x 109/mm3
boolean
C0032181 (UMLS CUI [1])
Life Expectancy
Item
patient life expectancy < 1 year
boolean
C0023671 (UMLS CUI [1])
Hypersensitivity clopidogrel | Aspirin allergy | Heparin allergy | Hypersensitivity Stainless Steel | Allergy to intravenous contrast media | Hypersensitivity Drug-Eluting Stents
Item
known allergies to clopidogrel, aspirin, heparin, stainless steel, iv contrast or stent drug elutant
boolean
C0020517 (UMLS CUI [1,1])
C0070166 (UMLS CUI [1,2])
C0004058 (UMLS CUI [2])
C0571776 (UMLS CUI [3])
C0020517 (UMLS CUI [4,1])
C0038126 (UMLS CUI [4,2])
C2242530 (UMLS CUI [5])
C0020517 (UMLS CUI [6,1])
C1322815 (UMLS CUI [6,2])
Gastrointestinal Hemorrhage Major
Item
recent major gi haemorrhage (within 3 months)
boolean
C0017181 (UMLS CUI [1,1])
C0205164 (UMLS CUI [1,2])
Cerebral Hemorrhage Episode
Item
any previous cerebral bleeding episode
boolean
C2937358 (UMLS CUI [1,1])
C0332189 (UMLS CUI [1,2])
Study Subject Participation Status | Investigational New Drugs | Investigational Medical Device
Item
participation in another investigational drug or device study
boolean
C2348568 (UMLS CUI [1])
C0013230 (UMLS CUI [2])
C2346570 (UMLS CUI [3])
Informed Consent Unable
Item
patient unable to give consent
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
Clinical decision Excludes Drug-Eluting Stent
Item
clinical decision precluding the use of drug eluting stent
boolean
C3845884 (UMLS CUI [1,1])
C0332196 (UMLS CUI [1,2])
C1322815 (UMLS CUI [1,3])
Retour au début de la page 

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