ID

19965

Descripción

Supplemental Benefit of Angiotensin Receptor Blocker in Hypertensive Patients With Stable Heart Failure Using Olmesartan; ODM derived from: https://clinicaltrials.gov/show/NCT00417222

Link

https://clinicaltrials.gov/show/NCT00417222

Palabras clave

Versiones (1)
  1. 1/2/17 1/2/17 -
Subido en

1 de febrero de 2017

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 Chronic Heart Failure NCT00417222

Inglés

Eligibility Chronic Heart Failure NCT00417222

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients who meet all of the following criteria.
Descripción

criteria Fulfill

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0243161
UMLS CUI [1,2]
C1550543
patients with nyha class ii through iv chronic heart failure.
Descripción

Chronic heart failure New York Heart Association Classification

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0264716
UMLS CUI [1,2]
C1275491
patients who have a history of hypertension or those who have antihypertensive medications.
Descripción

Hypertensive disease | Antihypertensive Agents

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0020538
UMLS CUI [2]
C0003364
patients who are aged 20 years or older and less than 80 years at the entry.
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
stable patients who have angiotensin converting enzyme inhibitor and/or beta-blocker.
Descripción

Angiotensin-Converting Enzyme Inhibitors | Adrenergic beta-Antagonists

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0003015
UMLS CUI [2]
C0001645
patients who do not have angiotensin ii receptor blocker.
Descripción

Angiotensin II receptor antagonist Absent

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0521942
UMLS CUI [1,2]
C0332197
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients who have renal dysfunction (serum creatinine >=3.0mg/dl) or those who are receiving chronic hemodialysis.
Descripción

Renal dysfunction | Creatinine measurement, serum | Chronic haemodialysis

Tipo de datos

boolean

Alias
UMLS CUI [1]
C3279454
UMLS CUI [2]
C0201976
UMLS CUI [3]
C1740835
history of drug hypersensitivity to olmesartan.
Descripción

Hypersensitivity olmesartan

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C1098320
patients who have severe liver dysfunction.
Descripción

Liver Dysfunction Severe

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0086565
UMLS CUI [1,2]
C0205082
history of angioedema.
Descripción

Angioedema

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0002994
history of malignant tumor or life-threatening illness of poor prognosis.
Descripción

Malignant Neoplasms | Life threatening illness Prognosis bad

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0006826
UMLS CUI [2,1]
C3846017
UMLS CUI [2,2]
C0278252
pregnant or possibly pregnant patients.
Descripción

Pregnancy | Possible pregnancy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0425965
cardiovascular surgery within 6months prior to the date of the entry.
Descripción

Cardiovascular Surgical Procedure

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0038897
acute myocardial infarction within 6 months prior to the date of the entry.
Descripción

Myocardial Infarction

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0027051
percutaneous coronary intervention or stent implantation within 6 months prior to the date of the entry.
Descripción

Percutaneous Coronary Intervention | Stenting

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1532338
UMLS CUI [2]
C2348535
other patients deemed unsuitable as subjects of the study by the treating physician.
Descripción

Study Subject Participation Status Inappropriate

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C1548788
Volver a la parte superior de la página

Similar models

Eligibility Chronic Heart Failure NCT00417222

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
criteria Fulfill
Item
patients who meet all of the following criteria.
boolean
C0243161 (UMLS CUI [1,1])
C1550543 (UMLS CUI [1,2])
Chronic heart failure New York Heart Association Classification
Item
patients with nyha class ii through iv chronic heart failure.
boolean
C0264716 (UMLS CUI [1,1])
C1275491 (UMLS CUI [1,2])
Hypertensive disease | Antihypertensive Agents
Item
patients who have a history of hypertension or those who have antihypertensive medications.
boolean
C0020538 (UMLS CUI [1])
C0003364 (UMLS CUI [2])
Age
Item
patients who are aged 20 years or older and less than 80 years at the entry.
boolean
C0001779 (UMLS CUI [1])
Angiotensin-Converting Enzyme Inhibitors | Adrenergic beta-Antagonists
Item
stable patients who have angiotensin converting enzyme inhibitor and/or beta-blocker.
boolean
C0003015 (UMLS CUI [1])
C0001645 (UMLS CUI [2])
Angiotensin II receptor antagonist Absent
Item
patients who do not have angiotensin ii receptor blocker.
boolean
C0521942 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Renal dysfunction | Creatinine measurement, serum | Chronic haemodialysis
Item
patients who have renal dysfunction (serum creatinine >=3.0mg/dl) or those who are receiving chronic hemodialysis.
boolean
C3279454 (UMLS CUI [1])
C0201976 (UMLS CUI [2])
C1740835 (UMLS CUI [3])
Hypersensitivity olmesartan
Item
history of drug hypersensitivity to olmesartan.
boolean
C0020517 (UMLS CUI [1,1])
C1098320 (UMLS CUI [1,2])
Liver Dysfunction Severe
Item
patients who have severe liver dysfunction.
boolean
C0086565 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
Angioedema
Item
history of angioedema.
boolean
C0002994 (UMLS CUI [1])
Malignant Neoplasms | Life threatening illness Prognosis bad
Item
history of malignant tumor or life-threatening illness of poor prognosis.
boolean
C0006826 (UMLS CUI [1])
C3846017 (UMLS CUI [2,1])
C0278252 (UMLS CUI [2,2])
Pregnancy | Possible pregnancy
Item
pregnant or possibly pregnant patients.
boolean
C0032961 (UMLS CUI [1])
C0425965 (UMLS CUI [2])
Cardiovascular Surgical Procedure
Item
cardiovascular surgery within 6months prior to the date of the entry.
boolean
C0038897 (UMLS CUI [1])
Myocardial Infarction
Item
acute myocardial infarction within 6 months prior to the date of the entry.
boolean
C0027051 (UMLS CUI [1])
Percutaneous Coronary Intervention | Stenting
Item
percutaneous coronary intervention or stent implantation within 6 months prior to the date of the entry.
boolean
C1532338 (UMLS CUI [1])
C2348535 (UMLS CUI [2])
Study Subject Participation Status Inappropriate
Item
other patients deemed unsuitable as subjects of the study by the treating physician.
boolean
C2348568 (UMLS CUI [1,1])
C1548788 (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