ID

28556

Descripción

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

Link

https://clinicaltrials.gov/show/NCT00794014

Palabras clave

Versiones (1)
  1. 22/1/18 22/1/18 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

22 de enero de 2018

DOI

Para solicitar uno, por favor iniciar sesión.

Licencia

Creative Commons BY 4.0
Comentarios del modelo :

Puede comentar sobre el modelo de datos aquí. A través de las burbujas de diálogo en los grupos de elementos y elementos, puede agregar comentarios específicos.

Volver a los comentarios del modelo
Comentarios de grupo de elementos para :

Comentarios del elemento para :

Para descargar modelos de datos, debe haber iniciado sesión. Por favor iniciar sesión o Registrate gratis.

Eligibility Coronary Artery Disease NCT00794014

Inglés

Eligibility Coronary Artery Disease NCT00794014

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

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

Parent vessel Percent Diameter Stenosis Measurement

Tipo de datos

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
Descripción

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

Tipo de datos

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
Descripción

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

Tipo de datos

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
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
cardiogenic shock
Descripción

Shock, Cardiogenic

Tipo de datos

boolean

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

ST segment elevation myocardial infarction

Tipo de datos

boolean

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

Ventricular Dysfunction, Left | Left ventricular ejection fraction Echocardiography

Tipo de datos

boolean

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

Vessel graft implant

Tipo de datos

boolean

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

Clopidogrel Due to Other medical condition

Tipo de datos

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
Descripción

Warfarin | cilostazol | Antiplatelet therapy

Tipo de datos

boolean

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

Hypersensitivity Clopidogrel | Aspirin allergy

Tipo de datos

boolean

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

Survival time Expected

Tipo de datos

boolean

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

Pregnancy, Planned

Tipo de datos

boolean

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

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

Tipo de datos

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.
Descripción

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

Tipo de datos

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
Volver a la parte superior de la página

Similar models

Eligibility Coronary Artery Disease NCT00794014

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
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])
Volver a la parte superior de la página 

Contacto

Utilice este formulario para comentarios, preguntas y sugerencias.

Los campos marcados con * son obligatorios.

Ayuda

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial