ID

29471

Descripción

Safety and Efficacy Study of Add On Aliskiren in Patients With Heart Failure and Renal Impairment; ODM derived from: https://clinicaltrials.gov/show/NCT00881439

Link

https://clinicaltrials.gov/show/NCT00881439

Palabras clave

Versiones (1)
  1. 29/3/18 29/3/18 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

29 de marzo 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 Heart Failure NCT00881439

Inglés

Eligibility Heart Failure NCT00881439

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
nyha ii-iv heart failure
Descripción

Heart failure New York Heart Association Classification

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0018801
UMLS CUI [1,2]
C1275491
left ventricular ejection fraction < 45%
Descripción

Left ventricular ejection fraction

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0428772
stable heart failure medication
Descripción

Pharmaceutical Preparations Stable Heart failure

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0205360
UMLS CUI [1,3]
C0018801
egfr by smdrd formula between 30 and 60 ml/min/1.73m2
Descripción

GFR estimation by MDRD

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2170215
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
known hypersensitivity to study drug or acei
Descripción

Hypersensitivity Investigational New Drugs | Angiotensin-converting-enzyme inhibitor allergy

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0013230
UMLS CUI [2]
C0571939
concomitant treatment with both arb and aldosterone receptor antagonist
Descripción

Angiotensin II receptor antagonist | Mineralocorticoid Receptor Antagonists

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0521942
UMLS CUI [2]
C1579268
symptomatic hypotension
Descripción

Hypotension symptomatic

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0863113
acute heart failure
Descripción

Acute heart failure

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0264714
history of stroke, acute coronary syndrome, pci or angioplasty within past 3 months
Descripción

Cerebrovascular accident | Acute Coronary Syndrome | Percutaneous Coronary Intervention | Angioplasty

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0038454
UMLS CUI [2]
C0948089
UMLS CUI [3]
C1532338
UMLS CUI [4]
C0162577
serum potassium > 5.2 mmol/l
Descripción

Serum potassium measurement

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0302353
right heart failure due to severe pulmonary disease
Descripción

Right Heart Failure Due to Lung disease Severe

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0235527
UMLS CUI [1,2]
C0678226
UMLS CUI [1,3]
C0024115
UMLS CUI [1,4]
C0205082
other protocol-defined inclusion/exclusion criteria may apply
Descripción

Eligibility Criteria Study Protocol

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1516637
UMLS CUI [1,2]
C2348563
Volver a la parte superior de la página

Similar models

Eligibility Heart Failure NCT00881439

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Heart failure New York Heart Association Classification
Item
nyha ii-iv heart failure
boolean
C0018801 (UMLS CUI [1,1])
C1275491 (UMLS CUI [1,2])
Left ventricular ejection fraction
Item
left ventricular ejection fraction < 45%
boolean
C0428772 (UMLS CUI [1])
Pharmaceutical Preparations Stable Heart failure
Item
stable heart failure medication
boolean
C0013227 (UMLS CUI [1,1])
C0205360 (UMLS CUI [1,2])
C0018801 (UMLS CUI [1,3])
GFR estimation by MDRD
Item
egfr by smdrd formula between 30 and 60 ml/min/1.73m2
boolean
C2170215 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Hypersensitivity Investigational New Drugs | Angiotensin-converting-enzyme inhibitor allergy
Item
known hypersensitivity to study drug or acei
boolean
C0020517 (UMLS CUI [1,1])
C0013230 (UMLS CUI [1,2])
C0571939 (UMLS CUI [2])
Angiotensin II receptor antagonist | Mineralocorticoid Receptor Antagonists
Item
concomitant treatment with both arb and aldosterone receptor antagonist
boolean
C0521942 (UMLS CUI [1])
C1579268 (UMLS CUI [2])
Hypotension symptomatic
Item
symptomatic hypotension
boolean
C0863113 (UMLS CUI [1])
Acute heart failure
Item
acute heart failure
boolean
C0264714 (UMLS CUI [1])
Cerebrovascular accident | Acute Coronary Syndrome | Percutaneous Coronary Intervention | Angioplasty
Item
history of stroke, acute coronary syndrome, pci or angioplasty within past 3 months
boolean
C0038454 (UMLS CUI [1])
C0948089 (UMLS CUI [2])
C1532338 (UMLS CUI [3])
C0162577 (UMLS CUI [4])
Serum potassium measurement
Item
serum potassium > 5.2 mmol/l
boolean
C0302353 (UMLS CUI [1])
Right Heart Failure Due to Lung disease Severe
Item
right heart failure due to severe pulmonary disease
boolean
C0235527 (UMLS CUI [1,1])
C0678226 (UMLS CUI [1,2])
C0024115 (UMLS CUI [1,3])
C0205082 (UMLS CUI [1,4])
Eligibility Criteria Study Protocol
Item
other protocol-defined inclusion/exclusion criteria may apply
boolean
C1516637 (UMLS CUI [1,1])
C2348563 (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