Eligibility Chronic Heart Failure NCT00417222

Inclusion Criteria
Beschrijving

Inclusion Criteria

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

criteria Fulfill

Datatype

boolean

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

Chronic heart failure New York Heart Association Classification

Datatype

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.
Beschrijving

Hypertensive disease | Antihypertensive Agents

Datatype

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.
Beschrijving

Age

Datatype

boolean

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

Angiotensin-Converting Enzyme Inhibitors | Adrenergic beta-Antagonists

Datatype

boolean

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

Angiotensin II receptor antagonist Absent

Datatype

boolean

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

Exclusion Criteria

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

Renal dysfunction | Creatinine measurement, serum | Chronic haemodialysis

Datatype

boolean

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

Hypersensitivity olmesartan

Datatype

boolean

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

Liver Dysfunction Severe

Datatype

boolean

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

Angioedema

Datatype

boolean

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

Malignant Neoplasms | Life threatening illness Prognosis bad

Datatype

boolean

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

Pregnancy | Possible pregnancy

Datatype

boolean

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

Cardiovascular Surgical Procedure

Datatype

boolean

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

Myocardial Infarction

Datatype

boolean

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

Percutaneous Coronary Intervention | Stenting

Datatype

boolean

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

Study Subject Participation Status Inappropriate

Datatype

boolean

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C1548788

Similar models

Eligibility Chronic Heart Failure NCT00417222

Name
Type
Description | Question | Decode (Coded Value)
Datatype
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])