ID

28556

Description

Optimal Strategy for Side Branch Stenting in Coronary Bifurcation Lesion; ODM derived from: https://clinicaltrials.gov/show/NCT00794014

Lien

https://clinicaltrials.gov/show/NCT00794014

Mots-clés

Versions (1)
  1. 22/01/2018 22/01/2018 -
Détendeur de droits

See clinicaltrials.gov

Téléchargé le

22 janvier 2018

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0
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Eligibility Coronary Artery Disease NCT00794014

Anglais

Eligibility Coronary Artery Disease NCT00794014

1 Formulaires  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
parent vessel diameter stenosis > 75%
Description

Parent vessel Percent Diameter Stenosis Measurement

Type de données

boolean

Alias
UMLS CUI [1,1]
C1562887
UMLS CUI [1,2]
C3897965
parent vessel diameter stenosis 50% - 75% with angina and/or objective evidence of ischemia in the non-invasive stress test
Description

Parent vessel Percent Diameter Stenosis Measurement | Angina Pectoris Non-Invasive Cardiac Stress Test | Ischemia Non-Invasive Cardiac Stress Test

Type de données

boolean

Alias
UMLS CUI [1,1]
C1562887
UMLS CUI [1,2]
C3897965
UMLS CUI [2,1]
C0002962
UMLS CUI [2,2]
C3272313
UMLS CUI [3,1]
C0022116
UMLS CUI [3,2]
C3272313
the reference diameter of both branches more than 2.3 mm by visual estimation
Description

Reference Diameter Size Branch of left coronary artery | Reference Diameter Size Branch of right coronary artery

Type de données

boolean

Alias
UMLS CUI [1,1]
C1706462
UMLS CUI [1,2]
C1301886
UMLS CUI [1,3]
C0456389
UMLS CUI [1,4]
C0447055
UMLS CUI [2,1]
C1706462
UMLS CUI [2,2]
C1301886
UMLS CUI [2,3]
C0456389
UMLS CUI [2,4]
C0447064
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
cardiogenic shock
Description

Shock, Cardiogenic

Type de données

boolean

Alias
UMLS CUI [1]
C0036980
st-elevation myocardial infarction within 48 hours of symptom onset
Description

ST segment elevation myocardial infarction

Type de données

boolean

Alias
UMLS CUI [1]
C1536220
left ventricular dysfunction (echocardiographic left ventricular ejection fraction < 25%)
Description

Ventricular Dysfunction, Left | Left ventricular ejection fraction Echocardiography

Type de données

boolean

Alias
UMLS CUI [1]
C0242698
UMLS CUI [2,1]
C0428772
UMLS CUI [2,2]
C0013516
graft vessels
Description

Vessel graft implant

Type de données

boolean

Alias
UMLS CUI [1]
C0565007
patients who have to receive clopidogrel due to other conditions
Description

Clopidogrel Due to Other medical condition

Type de données

boolean

Alias
UMLS CUI [1,1]
C0070166
UMLS CUI [1,2]
C0678226
UMLS CUI [1,3]
C3843040
patients who have to receive warfarin, cilostazol or other antiplatelet therapy
Description

Warfarin | cilostazol | Antiplatelet therapy

Type de données

boolean

Alias
UMLS CUI [1]
C0043031
UMLS CUI [2]
C0055729
UMLS CUI [3]
C1096021
hypersensitivity to clopidogrel or aspirin
Description

Hypersensitivity Clopidogrel | Aspirin allergy

Type de données

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0070166
UMLS CUI [2]
C0004058
expectant survival less than 1 year
Description

Survival time Expected

Type de données

boolean

Alias
UMLS CUI [1,1]
C2919552
UMLS CUI [1,2]
C1517001
women who plan to become pregnant
Description

Pregnancy, Planned

Type de données

boolean

Alias
UMLS CUI [1]
C0032992
patients with bleeding diathesis (coagulopathy, thrombocytopenia or platelet dysfunction, gastrointestinal or genitourinary bleeding within the prior 3 months)
Description

Bleeding tendency | Blood Coagulation Disorders | Thrombocytopenia | Platelet dysfunction | Gastrointestinal Hemorrhage | Genitourinary tract hemorrhage

Type de données

boolean

Alias
UMLS CUI [1]
C1458140
UMLS CUI [2]
C0005779
UMLS CUI [3]
C0040034
UMLS CUI [4]
C0679429
UMLS CUI [5]
C0017181
UMLS CUI [6]
C0919591
patients who are actively participating in another drug or device investigational study, which have not completed the primary endpoint follow-up period.
Description

Study Subject Participation Status | Investigational New Drugs | Investigational Medical Device | Primary Endpoint Follow-up Incomplete

Type de données

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2]
C0013230
UMLS CUI [3]
C2346570
UMLS CUI [4,1]
C2986535
UMLS CUI [4,2]
C3274571
UMLS CUI [4,3]
C0205257
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Similar models

Eligibility Coronary Artery Disease NCT00794014

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Parent vessel Percent Diameter Stenosis Measurement
Item
parent vessel diameter stenosis > 75%
boolean
C1562887 (UMLS CUI [1,1])
C3897965 (UMLS CUI [1,2])
Parent vessel Percent Diameter Stenosis Measurement | Angina Pectoris Non-Invasive Cardiac Stress Test | Ischemia Non-Invasive Cardiac Stress Test
Item
parent vessel diameter stenosis 50% - 75% with angina and/or objective evidence of ischemia in the non-invasive stress test
boolean
C1562887 (UMLS CUI [1,1])
C3897965 (UMLS CUI [1,2])
C0002962 (UMLS CUI [2,1])
C3272313 (UMLS CUI [2,2])
C0022116 (UMLS CUI [3,1])
C3272313 (UMLS CUI [3,2])
Reference Diameter Size Branch of left coronary artery | Reference Diameter Size Branch of right coronary artery
Item
the reference diameter of both branches more than 2.3 mm by visual estimation
boolean
C1706462 (UMLS CUI [1,1])
C1301886 (UMLS CUI [1,2])
C0456389 (UMLS CUI [1,3])
C0447055 (UMLS CUI [1,4])
C1706462 (UMLS CUI [2,1])
C1301886 (UMLS CUI [2,2])
C0456389 (UMLS CUI [2,3])
C0447064 (UMLS CUI [2,4])
Item Group
C0680251 (UMLS CUI)
Shock, Cardiogenic
Item
cardiogenic shock
boolean
C0036980 (UMLS CUI [1])
ST segment elevation myocardial infarction
Item
st-elevation myocardial infarction within 48 hours of symptom onset
boolean
C1536220 (UMLS CUI [1])
Ventricular Dysfunction, Left | Left ventricular ejection fraction Echocardiography
Item
left ventricular dysfunction (echocardiographic left ventricular ejection fraction < 25%)
boolean
C0242698 (UMLS CUI [1])
C0428772 (UMLS CUI [2,1])
C0013516 (UMLS CUI [2,2])
Vessel graft implant
Item
graft vessels
boolean
C0565007 (UMLS CUI [1])
Clopidogrel Due to Other medical condition
Item
patients who have to receive clopidogrel due to other conditions
boolean
C0070166 (UMLS CUI [1,1])
C0678226 (UMLS CUI [1,2])
C3843040 (UMLS CUI [1,3])
Warfarin | cilostazol | Antiplatelet therapy
Item
patients who have to receive warfarin, cilostazol or other antiplatelet therapy
boolean
C0043031 (UMLS CUI [1])
C0055729 (UMLS CUI [2])
C1096021 (UMLS CUI [3])
Hypersensitivity Clopidogrel | Aspirin allergy
Item
hypersensitivity to clopidogrel or aspirin
boolean
C0020517 (UMLS CUI [1,1])
C0070166 (UMLS CUI [1,2])
C0004058 (UMLS CUI [2])
Survival time Expected
Item
expectant survival less than 1 year
boolean
C2919552 (UMLS CUI [1,1])
C1517001 (UMLS CUI [1,2])
Pregnancy, Planned
Item
women who plan to become pregnant
boolean
C0032992 (UMLS CUI [1])
Bleeding tendency | Blood Coagulation Disorders | Thrombocytopenia | Platelet dysfunction | Gastrointestinal Hemorrhage | Genitourinary tract hemorrhage
Item
patients with bleeding diathesis (coagulopathy, thrombocytopenia or platelet dysfunction, gastrointestinal or genitourinary bleeding within the prior 3 months)
boolean
C1458140 (UMLS CUI [1])
C0005779 (UMLS CUI [2])
C0040034 (UMLS CUI [3])
C0679429 (UMLS CUI [4])
C0017181 (UMLS CUI [5])
C0919591 (UMLS CUI [6])
Study Subject Participation Status | Investigational New Drugs | Investigational Medical Device | Primary Endpoint Follow-up Incomplete
Item
patients who are actively participating in another drug or device investigational study, which have not completed the primary endpoint follow-up period.
boolean
C2348568 (UMLS CUI [1])
C0013230 (UMLS CUI [2])
C2346570 (UMLS CUI [3])
C2986535 (UMLS CUI [4,1])
C3274571 (UMLS CUI [4,2])
C0205257 (UMLS CUI [4,3])
Retour au début de la page 

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