ID

15920

Descripción

POISE Trial: Perioperative Ischemic Evaluation Study; ODM derived from: https://clinicaltrials.gov/show/NCT00182039

Link

https://clinicaltrials.gov/show/NCT00182039

Palabras clave

Versiones (2)
  1. 5/6/16 5/6/16 -
  2. 18/6/16 18/6/16 -
Subido en

18 de junio de 2016

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 Cardiovascular Diseases NCT00182039

Inglés

Eligibility Cardiovascular Diseases NCT00182039

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients undergoing noncardiac surgery
Descripción

noncardiac surgery

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0543467
UMLS CUI [1,2]
C1522601
UMLS CUI [1,3]
C1518422
≥ 45 years of age; either sex.
Descripción

age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
have an expected length of stay ≥ 24 hours
Descripción

in-patient duration

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0023303
fulfill any one of the following 6 criteria:
Descripción

ID.4

Tipo de datos

boolean

coronary artery disease;
Descripción

coronary artery disease

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1956346
peripheral vascular disease;
Descripción

peripheral vascular disease

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0085096
history of stroke due to atherothrombotic disease;
Descripción

history of stroke

Tipo de datos

boolean

Alias
UMLS CUI [1]
C4039739
hospitalization for congestive heart failure within 3 years of randomization;
Descripción

congestive heart failure

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0019993
UMLS CUI [1,2]
C0018802
undergoing major vascular surgery; or
Descripción

major vascular surgery

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0042381
any 3 of the following 7 criteria: scheduled for high risk surgery (i.e. intraperitoneal or intrathoracic); emergency/urgent surgery; any history of congestive heart failure; history of a transient ischemic attack (tia); diabetes and currently on an oral hypoglycemic agent or insulin therapy; preoperative serum creatinine > 175 µmol/l (> 2.0 mg/dl); or age > 70 years.
Descripción

informed consent; comorbidities

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2216322
UMLS CUI [2,1]
C0018802
UMLS CUI [2,2]
C0262926
UMLS CUI [3,1]
C0007787
UMLS CUI [3,2]
C0262926
UMLS CUI [4,1]
C0011849
UMLS CUI [4,2]
C0020616
UMLS CUI [4,3]
C0557978
UMLS CUI [5,1]
C0201976
UMLS CUI [5,2]
C0445204
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
contraindication to metoprolol including any of the following: significant bradycardia (heart rate < 50 beats per minute); second or third degree heart block without a pacemaker; asthma that has been active within the last decade; and history of chronic obstructive pulmonary disease (copd) with bronchospasm on pulmonary function tests.
Descripción

contraindication to metoprolol

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0428977
UMLS CUI [2]
C0264906
UMLS CUI [3]
C0151517
UMLS CUI [4]
C0004096
UMLS CUI [5]
C0024117
clinical plan to use a beta-blocker preoperatively or during the first 30 postoperative days
Descripción

beta-blocker usage

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001645
prior adverse reaction to a beta-blocker
Descripción

hypersensitivity to beta-blocker

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0001645
coronary artery bypass graft (cabg) surgery with complete revascularization in the preceding 5 years and no evidence of cardiac ischemia since the cabg surgery
Descripción

cabg

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0010055
UMLS CUI [1,2]
C0151744
UMLS CUI [1,3]
C0332197
patients undergoing low risk surgical procedures (potential examples include transurethral procedures [transurethral prostatectomies (turps), stone baskets, etc.], ophthalmologic procedures under topical or regional anesthesia [cornea transplants, cataract surgery, etc.], and surgeries with limited physiological stresses [digital re-implantation, nerve repairs, etc.] )
Descripción

low risk surgery

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0543467
UMLS CUI [1,2]
C3538919
concurrent use of verapamil
Descripción

concurrent use of verapamil

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0009429
UMLS CUI [1,2]
C0042523
prior enrollment in this trial
Descripción

prior enrollment in this trial

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1516879
UMLS CUI [1,2]
C0332152
Volver a la parte superior de la página

Similar models

Eligibility Cardiovascular Diseases NCT00182039

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
noncardiac surgery
Item
patients undergoing noncardiac surgery
boolean
C0543467 (UMLS CUI [1,1])
C1522601 (UMLS CUI [1,2])
C1518422 (UMLS CUI [1,3])
age
Item
≥ 45 years of age; either sex.
boolean
C0001779 (UMLS CUI [1])
in-patient duration
Item
have an expected length of stay ≥ 24 hours
boolean
C0023303 (UMLS CUI [1])
ID.4
Item
fulfill any one of the following 6 criteria:
boolean
coronary artery disease
Item
coronary artery disease;
boolean
C1956346 (UMLS CUI [1])
peripheral vascular disease
Item
peripheral vascular disease;
boolean
C0085096 (UMLS CUI [1])
history of stroke
Item
history of stroke due to atherothrombotic disease;
boolean
C4039739 (UMLS CUI [1])
congestive heart failure
Item
hospitalization for congestive heart failure within 3 years of randomization;
boolean
C0019993 (UMLS CUI [1,1])
C0018802 (UMLS CUI [1,2])
major vascular surgery
Item
undergoing major vascular surgery; or
boolean
C0042381 (UMLS CUI [1])
informed consent; comorbidities
Item
any 3 of the following 7 criteria: scheduled for high risk surgery (i.e. intraperitoneal or intrathoracic); emergency/urgent surgery; any history of congestive heart failure; history of a transient ischemic attack (tia); diabetes and currently on an oral hypoglycemic agent or insulin therapy; preoperative serum creatinine > 175 µmol/l (> 2.0 mg/dl); or age > 70 years.
boolean
C2216322 (UMLS CUI [1])
C0018802 (UMLS CUI [2,1])
C0262926 (UMLS CUI [2,2])
C0007787 (UMLS CUI [3,1])
C0262926 (UMLS CUI [3,2])
C0011849 (UMLS CUI [4,1])
C0020616 (UMLS CUI [4,2])
C0557978 (UMLS CUI [4,3])
C0201976 (UMLS CUI [5,1])
C0445204 (UMLS CUI [5,2])
Item Group
C0680251 (UMLS CUI)
contraindication to metoprolol
Item
contraindication to metoprolol including any of the following: significant bradycardia (heart rate < 50 beats per minute); second or third degree heart block without a pacemaker; asthma that has been active within the last decade; and history of chronic obstructive pulmonary disease (copd) with bronchospasm on pulmonary function tests.
boolean
C0428977 (UMLS CUI [1])
C0264906 (UMLS CUI [2])
C0151517 (UMLS CUI [3])
C0004096 (UMLS CUI [4])
C0024117 (UMLS CUI [5])
beta-blocker usage
Item
clinical plan to use a beta-blocker preoperatively or during the first 30 postoperative days
boolean
C0001645 (UMLS CUI [1])
hypersensitivity to beta-blocker
Item
prior adverse reaction to a beta-blocker
boolean
C0020517 (UMLS CUI [1,1])
C0001645 (UMLS CUI [1,2])
cabg
Item
coronary artery bypass graft (cabg) surgery with complete revascularization in the preceding 5 years and no evidence of cardiac ischemia since the cabg surgery
boolean
C0010055 (UMLS CUI [1,1])
C0151744 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
low risk surgery
Item
patients undergoing low risk surgical procedures (potential examples include transurethral procedures [transurethral prostatectomies (turps), stone baskets, etc.], ophthalmologic procedures under topical or regional anesthesia [cornea transplants, cataract surgery, etc.], and surgeries with limited physiological stresses [digital re-implantation, nerve repairs, etc.] )
boolean
C0543467 (UMLS CUI [1,1])
C3538919 (UMLS CUI [1,2])
concurrent use of verapamil
Item
concurrent use of verapamil
boolean
C0009429 (UMLS CUI [1,1])
C0042523 (UMLS CUI [1,2])
prior enrollment in this trial
Item
prior enrollment in this trial
boolean
C1516879 (UMLS CUI [1,1])
C0332152 (UMLS CUI [1,2])
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