ID

39384

Descripción

The SMARTEX Heart Failure Study; ODM derived from: https://clinicaltrials.gov/show/NCT00917046

Link

https://clinicaltrials.gov/show/NCT00917046

Palabras clave

Versiones (1)
  1. 5/1/20 5/1/20 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

5 de enero de 2020

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 Heart Failure NCT00917046

Inglés

Eligibility Heart Failure NCT00917046

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
congestive heart failure after myocardial infarction or dilated cardiomyopathy with:
Descripción

Congestive heart failure | Status post Myocardial Infarction | Status post Dilated Cardiomyopathy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0018802
UMLS CUI [2,1]
C0231290
UMLS CUI [2,2]
C0027051
UMLS CUI [3,1]
C0231290
UMLS CUI [3,2]
C0007193
lvef < 0.35,
Descripción

Left ventricular ejection fraction

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0428772
nyha class ii - iii,
Descripción

New York Heart Association Classification

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1275491
stable without any signs of worsening for at least 6 weeks,
Descripción

Stable status | Worsening pattern Absent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0205360
UMLS CUI [2,1]
C0332271
UMLS CUI [2,2]
C0332197
minimum 3 months of optimal medical treatment,
Descripción

Therapy Optimal

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C2698651
previous revascularisation or crt should be more than 6 months before inclusion.
Descripción

Revascularization Previous | Cardiac Resynchronization Therapy Previous

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0581603
UMLS CUI [1,2]
C0205156
UMLS CUI [2,1]
C1167956
UMLS CUI [2,2]
C0205156
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
significant intercurrent illness last 6 weeks,
Descripción

Comorbidity Significant

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C0750502
known severe ventricular arrhythmia with functional or prognostic significance unless protected with icd,
Descripción

Ventricular arrhythmia Severe

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0085612
UMLS CUI [1,2]
C0205082
significant ischemia,
Descripción

Ischemia

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0022116
hemodynamic deterioration or exercise-induced arrhythmia at baseline testing,
Descripción

Hemodynamics deterioration | Cardiac Arrhythmia Exercise induced

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0019010
UMLS CUI [1,2]
C0868945
UMLS CUI [2,1]
C0003811
UMLS CUI [2,2]
C0239313
other heart disease that limits exercise tolerance (valve disease with significant hemodynamic consequences, hypertrophic cardiomyopathy etc.,
Descripción

Heart Disease Limiting Exercise Tolerance | Valvular disease | Hypertrophic Cardiomyopathy

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0018799
UMLS CUI [1,2]
C0439801
UMLS CUI [1,3]
C0162521
UMLS CUI [2]
C3258293
UMLS CUI [3]
C0007194
co-morbidity that may significantly influence one-year prognosis,
Descripción

Comorbidity Influence Prognosis

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C4054723
UMLS CUI [1,3]
C0033325
functional or mental disability that may limit exercise,
Descripción

Functional disability Limiting Exercise | Mental handicap Limiting Exercise

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0872173
UMLS CUI [1,2]
C0439801
UMLS CUI [1,3]
C0015259
UMLS CUI [2,1]
C1306341
UMLS CUI [2,2]
C0439801
UMLS CUI [2,3]
C0015259
patients scheduled for heart transplant at time of inclusion,
Descripción

Heart Transplantation Scheduled

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0018823
UMLS CUI [1,2]
C0205539
a habit of regular vigorous exercise or participation in a program of exercise training less than 6 months before inclusion, or participation in another clinical trial,
Descripción

Vigorous physical activity | Exercise Training | Study Subject Participation Status | Clinical Trial

Tipo de datos

boolean

Alias
UMLS CUI [1]
C4267713
UMLS CUI [2]
C4279936
UMLS CUI [3]
C2348568
UMLS CUI [4]
C0008976
patients with copd with fev1 below 50% of expected values are excluded,
Descripción

Chronic Obstructive Airway Disease | Percent predicted FEV1

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0024117
UMLS CUI [2]
C0730561
patients taking oral corticosteroids are excluded in all cases.
Descripción

Adrenal Cortex Hormones Oral

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0001617
UMLS CUI [1,2]
C1527415
Volver a la parte superior de la página

Similar models

Eligibility Heart Failure NCT00917046

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Congestive heart failure | Status post Myocardial Infarction | Status post Dilated Cardiomyopathy
Item
congestive heart failure after myocardial infarction or dilated cardiomyopathy with:
boolean
C0018802 (UMLS CUI [1])
C0231290 (UMLS CUI [2,1])
C0027051 (UMLS CUI [2,2])
C0231290 (UMLS CUI [3,1])
C0007193 (UMLS CUI [3,2])
Left ventricular ejection fraction
Item
lvef < 0.35,
boolean
C0428772 (UMLS CUI [1])
New York Heart Association Classification
Item
nyha class ii - iii,
boolean
C1275491 (UMLS CUI [1])
Stable status | Worsening pattern Absent
Item
stable without any signs of worsening for at least 6 weeks,
boolean
C0205360 (UMLS CUI [1])
C0332271 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
Therapy Optimal
Item
minimum 3 months of optimal medical treatment,
boolean
C0087111 (UMLS CUI [1,1])
C2698651 (UMLS CUI [1,2])
Revascularization Previous | Cardiac Resynchronization Therapy Previous
Item
previous revascularisation or crt should be more than 6 months before inclusion.
boolean
C0581603 (UMLS CUI [1,1])
C0205156 (UMLS CUI [1,2])
C1167956 (UMLS CUI [2,1])
C0205156 (UMLS CUI [2,2])
Item Group
C0680251 (UMLS CUI)
Comorbidity Significant
Item
significant intercurrent illness last 6 weeks,
boolean
C0009488 (UMLS CUI [1,1])
C0750502 (UMLS CUI [1,2])
Ventricular arrhythmia Severe
Item
known severe ventricular arrhythmia with functional or prognostic significance unless protected with icd,
boolean
C0085612 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
Ischemia
Item
significant ischemia,
boolean
C0022116 (UMLS CUI [1])
Hemodynamics deterioration | Cardiac Arrhythmia Exercise induced
Item
hemodynamic deterioration or exercise-induced arrhythmia at baseline testing,
boolean
C0019010 (UMLS CUI [1,1])
C0868945 (UMLS CUI [1,2])
C0003811 (UMLS CUI [2,1])
C0239313 (UMLS CUI [2,2])
Heart Disease Limiting Exercise Tolerance | Valvular disease | Hypertrophic Cardiomyopathy
Item
other heart disease that limits exercise tolerance (valve disease with significant hemodynamic consequences, hypertrophic cardiomyopathy etc.,
boolean
C0018799 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0162521 (UMLS CUI [1,3])
C3258293 (UMLS CUI [2])
C0007194 (UMLS CUI [3])
Comorbidity Influence Prognosis
Item
co-morbidity that may significantly influence one-year prognosis,
boolean
C0009488 (UMLS CUI [1,1])
C4054723 (UMLS CUI [1,2])
C0033325 (UMLS CUI [1,3])
Functional disability Limiting Exercise | Mental handicap Limiting Exercise
Item
functional or mental disability that may limit exercise,
boolean
C0872173 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0015259 (UMLS CUI [1,3])
C1306341 (UMLS CUI [2,1])
C0439801 (UMLS CUI [2,2])
C0015259 (UMLS CUI [2,3])
Heart Transplantation Scheduled
Item
patients scheduled for heart transplant at time of inclusion,
boolean
C0018823 (UMLS CUI [1,1])
C0205539 (UMLS CUI [1,2])
Vigorous physical activity | Exercise Training | Study Subject Participation Status | Clinical Trial
Item
a habit of regular vigorous exercise or participation in a program of exercise training less than 6 months before inclusion, or participation in another clinical trial,
boolean
C4267713 (UMLS CUI [1])
C4279936 (UMLS CUI [2])
C2348568 (UMLS CUI [3])
C0008976 (UMLS CUI [4])
Chronic Obstructive Airway Disease | Percent predicted FEV1
Item
patients with copd with fev1 below 50% of expected values are excluded,
boolean
C0024117 (UMLS CUI [1])
C0730561 (UMLS CUI [2])
Adrenal Cortex Hormones Oral
Item
patients taking oral corticosteroids are excluded in all cases.
boolean
C0001617 (UMLS CUI [1,1])
C1527415 (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