ID

19965

Description

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

Keywords

Versions (1)
  1. 2/1/17 2/1/17 -
Uploaded on

February 1, 2017

DOI

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License

Creative Commons BY 4.0
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Eligibility Chronic Heart Failure NCT00417222

English

Eligibility Chronic Heart Failure NCT00417222

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

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

criteria Fulfill

Data type

boolean

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

Chronic heart failure New York Heart Association Classification

Data type

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.
Description

Hypertensive disease | Antihypertensive Agents

Data type

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.
Description

Age

Data type

boolean

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

Angiotensin-Converting Enzyme Inhibitors | Adrenergic beta-Antagonists

Data type

boolean

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

Angiotensin II receptor antagonist Absent

Data type

boolean

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

Exclusion Criteria

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

Renal dysfunction | Creatinine measurement, serum | Chronic haemodialysis

Data type

boolean

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

Hypersensitivity olmesartan

Data type

boolean

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

Liver Dysfunction Severe

Data type

boolean

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

Angioedema

Data type

boolean

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

Malignant Neoplasms | Life threatening illness Prognosis bad

Data type

boolean

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

Pregnancy | Possible pregnancy

Data type

boolean

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

Cardiovascular Surgical Procedure

Data type

boolean

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

Myocardial Infarction

Data type

boolean

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

Percutaneous Coronary Intervention | Stenting

Data type

boolean

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

Study Subject Participation Status Inappropriate

Data type

boolean

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

Eligibility Chronic Heart Failure NCT00417222

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
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])
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