ID

11715

Descripción

This study will compare the effect of a prasugrel 10-mg maintenance dose with a clopidogrel 75-mg maintenance dose on platelet activity, approximately 1 week after the first dose of study drug, in subjects who have been taking clopidogrel 75 mg daily following a percutaneous coronary intervention (PCI) with placement of a stent, performed to treat acute coronary syndrome (ACS). https://clinicaltrials.gov/ct2/show/NCT00356135

Link

https://clinicaltrials.gov/ct2/show/NCT00356135

Palabras clave

Versiones (1)
  1. 28/7/15 28/7/15 -
Subido en

28 de julio de 2015

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 SWAP Acute Coronary Syndrome NCT00356135

Inglés

Eligibility Criteria

1 formularios  
  1. StudyEvent: ODM
    1. Eligibility Criteria
Inclusion Criteria
Descripción

Inclusion Criteria

Present with a recent history of an ACS event
Descripción

Present with a recent history of an ACS event

Tipo de datos

boolean

Alias
UMLS CUI-1
C0948089
who state that they are supposed to be taking daily aspirin
Descripción

who state that they are supposed to be taking daily aspirin

Tipo de datos

boolean

Alias
UMLS CUI-1
C0004057
who state that they are supposed to be taking maintenance dose 75-mg clopidogrel.
Descripción

who state that they are supposed to be taking maintenance dose 75-mg clopidogrel.

Tipo de datos

boolean

Alias
UMLS CUI-1
C0070166
Are of a legal age (and at least 18 years of age but less than 75 years of age)
Descripción

Are of a legal age (and at least 18 years of age but less than 75 years of age)

Tipo de datos

boolean

Alias
UMLS CUI-1
C0001779
Are competent mental condition to provide written informed consent before entering the study.
Descripción

Are competent mental condition to provide written informed consent before entering the study.

Tipo de datos

boolean

Alias
UMLS CUI-1
C0021430
Exclusion Criteria
Descripción

Exclusion Criteria

Left main coronary artery stent
Descripción

Left main coronary artery stent

Tipo de datos

boolean

Alias
UMLS CUI-1
N
left anterior descending (LAD) bifurcation stent
Descripción

left anterior descending (LAD) bifurcation stent

Tipo de datos

boolean

Alias
UMLS CUI-1
C3836455
Have any form of coronary revascularization (percutaneous coronary intervention [PCI] or coronary artery bypass grafting [CABG]) planned to occur during the study (from signing consent through the final visit).
Descripción

Have any form of coronary revascularization (percutaneous coronary intervention [PCI] or coronary artery bypass grafting [CABG]) planned to occur during the study (from signing consent through the final visit).

Tipo de datos

boolean

Alias
UMLS CUI-1
C1532338
Have any form of coronary revascularization (percutaneous coronary intervention [PCI] or coronary artery bypass grafting [CABG]) planned to occur during the study (from signing consent through the final visit).
Descripción

Have any form of coronary revascularization (percutaneous coronary intervention [PCI] or coronary artery bypass grafting [CABG]) planned to occur during the study (from signing consent through the final visit).

Tipo de datos

boolean

Alias
UMLS CUI-1
C0010055
Receiving or will receive oral anticoagulation (other than aspirin and clopidogrel) that cannot be safely discontinued for the duration of the study.
Descripción

Receiving or will receive oral anticoagulation (other than aspirin and clopidogrel) that cannot be safely discontinued for the duration of the study.

Tipo de datos

boolean

Alias
UMLS CUI-1
C0354604
Receiving or will receive other antiplatelet therapy (other than aspirin and clopidogrel) that cannot be safely discontinued for the duration of the study.
Descripción

Receiving or will receive other antiplatelet therapy (other than aspirin and clopidogrel) that cannot be safely discontinued for the duration of the study.

Tipo de datos

boolean

Alias
UMLS CUI-1
C1096021
Receiving daily treatment with nonsteroidal anti-inflammatory drugs (NSAIDs) that cannot be discontinued or are anticipated to require daily treatment with NSAIDs during the study.
Descripción

Receiving daily treatment with nonsteroidal anti-inflammatory drugs (NSAIDs) that cannot be discontinued or are anticipated to require daily treatment with NSAIDs during the study.

Tipo de datos

boolean

Alias
UMLS CUI-1
C0003211
history of ischemic or hemorrhagic stroke
Descripción

history of ischemic or hemorrhagic stroke

Tipo de datos

boolean

Alias
UMLS CUI-1
C0559159
Intracranial neoplasm
Descripción

Intracranial neoplasm

Tipo de datos

boolean

Alias
UMLS CUI-1
C1527390
Arteriovenous malformation
Descripción

Arteriovenous malformation

Tipo de datos

boolean

Alias
UMLS CUI-1
C0003857
Aneurysm
Descripción

Aneurysm

Tipo de datos

boolean

Alias
UMLS CUI-1
C0002940
History of transient ischemic attack (TIA)
Descripción

History of transient ischemic attack (TIA)

Tipo de datos

boolean

Alias
UMLS CUI-1
C0455536
Have a body weight less than 60 kilograms (kg)
Descripción

Have a body weight less than 60 kilograms (kg)

Tipo de datos

boolean

Volver a la parte superior de la página

Similar models

Eligibility Criteria

1 formularios
  1. StudyEvent: ODM
    1. Eligibility Criteria
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Inclusion Criteria
Acute coronary syndrome
Item
Present with a recent history of an ACS event
boolean
C0948089 (UMLS CUI-1)
Aspirin
Item
who state that they are supposed to be taking daily aspirin
boolean
C0004057 (UMLS CUI-1)
Clopidogrel
Item
who state that they are supposed to be taking maintenance dose 75-mg clopidogrel.
boolean
C0070166 (UMLS CUI-1)
Age
Item
Are of a legal age (and at least 18 years of age but less than 75 years of age)
boolean
C0001779 (UMLS CUI-1)
Informed consent
Item
Are competent mental condition to provide written informed consent before entering the study.
boolean
C0021430 (UMLS CUI-1)
Item Group
Exclusion Criteria
Left main coronary artery stent
Item
Left main coronary artery stent
boolean
N (UMLS CUI-1)
left anterior descending (LAD) bifurcation stent
Item
left anterior descending (LAD) bifurcation stent
boolean
C3836455 (UMLS CUI-1)
PCI
Item
Have any form of coronary revascularization (percutaneous coronary intervention [PCI] or coronary artery bypass grafting [CABG]) planned to occur during the study (from signing consent through the final visit).
boolean
C1532338 (UMLS CUI-1)
CABG
Item
Have any form of coronary revascularization (percutaneous coronary intervention [PCI] or coronary artery bypass grafting [CABG]) planned to occur during the study (from signing consent through the final visit).
boolean
C0010055 (UMLS CUI-1)
Oral anticoagulants
Item
Receiving or will receive oral anticoagulation (other than aspirin and clopidogrel) that cannot be safely discontinued for the duration of the study.
boolean
C0354604 (UMLS CUI-1)
Antiplatelet therapy
Item
Receiving or will receive other antiplatelet therapy (other than aspirin and clopidogrel) that cannot be safely discontinued for the duration of the study.
boolean
C1096021 (UMLS CUI-1)
NSAID
Item
Receiving daily treatment with nonsteroidal anti-inflammatory drugs (NSAIDs) that cannot be discontinued or are anticipated to require daily treatment with NSAIDs during the study.
boolean
C0003211 (UMLS CUI-1)
History of stroke
Item
history of ischemic or hemorrhagic stroke
boolean
C0559159 (UMLS CUI-1)
Intracranial neoplasm
Item
Intracranial neoplasm
boolean
C1527390 (UMLS CUI-1)
Arteriovenous malformation
Item
Arteriovenous malformation
boolean
C0003857 (UMLS CUI-1)
Aneurysm
Item
Aneurysm
boolean
C0002940 (UMLS CUI-1)
History of TIA
Item
History of transient ischemic attack (TIA)
boolean
C0455536 (UMLS CUI-1)
Weight
Item
Have a body weight less than 60 kilograms (kg)
boolean
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