Eligibility Cardiovascular Disease NCT00846118

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients under hemodialysis
Description

Hemodialysis

Data type

boolean

Alias
UMLS CUI [1]
C0019004
patients with hypercholesterolemia as defined by any of following parameters:
Description

Hypercholesterolemia

Data type

boolean

Alias
UMLS CUI [1]
C0020443
ldl-c ≧ 100 mg / dl
Description

Low density lipoprotein cholesterol measurement

Data type

boolean

Alias
UMLS CUI [1]
C0202117
tc ≧ 180 mg / dl
Description

Serum total cholesterol measurement

Data type

boolean

Alias
UMLS CUI [1]
C1445957
patients required cholesterol-lowering treatment by investigators.
Description

Anticholesteremic Agents Patient need for

Data type

boolean

Alias
UMLS CUI [1,1]
C0003277
UMLS CUI [1,2]
C0686904
patients aged 20-75 years
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
patients with written consent by their own volition after being provided sufficient explanation for the participation into this clinical trial
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients taking statins or fibrates
Description

Statins | Fibrates

Data type

boolean

Alias
UMLS CUI [1]
C0360714
UMLS CUI [2]
C1449704
patients enrolled to the other trials using contraindication drugs of pitavastatin
Description

Study Subject Participation Status | Medical contraindication pitavastatin

Data type

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2,1]
C1301624
UMLS CUI [2,2]
C1101838
patients who had acute myocardial infarction within six months before the day of the agreement acquisition
Description

Myocardial Infarction

Data type

boolean

Alias
UMLS CUI [1]
C0027051
patients scheduled pci and cabg within six months after the day of the agreement acquisition
Description

Percutaneous Coronary Intervention Scheduled | Coronary Artery Bypass Surgery Scheduled

Data type

boolean

Alias
UMLS CUI [1,1]
C1532338
UMLS CUI [1,2]
C0205539
UMLS CUI [2,1]
C0010055
UMLS CUI [2,2]
C0205539
patients who had diagnosis or doubt of malignant tumor
Description

Malignant Neoplasms | Malignant Neoplasms Unlikely

Data type

boolean

Alias
UMLS CUI [1]
C0006826
UMLS CUI [2,1]
C0006826
UMLS CUI [2,2]
C0750558
patients corresponded to "contraindications" of pitavastatin
Description

Medical contraindication pitavastatin

Data type

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C1101838
familial hypercholesterolemia patients
Description

Hypercholesterolemia, Familial

Data type

boolean

Alias
UMLS CUI [1]
C0020445
patients judged ineligible by investigators
Description

Patients Ineligible

Data type

boolean

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C1512714

Similar models

Eligibility Cardiovascular Disease NCT00846118

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Hemodialysis
Item
patients under hemodialysis
boolean
C0019004 (UMLS CUI [1])
Hypercholesterolemia
Item
patients with hypercholesterolemia as defined by any of following parameters:
boolean
C0020443 (UMLS CUI [1])
Low density lipoprotein cholesterol measurement
Item
ldl-c ≧ 100 mg / dl
boolean
C0202117 (UMLS CUI [1])
Serum total cholesterol measurement
Item
tc ≧ 180 mg / dl
boolean
C1445957 (UMLS CUI [1])
Anticholesteremic Agents Patient need for
Item
patients required cholesterol-lowering treatment by investigators.
boolean
C0003277 (UMLS CUI [1,1])
C0686904 (UMLS CUI [1,2])
Age
Item
patients aged 20-75 years
boolean
C0001779 (UMLS CUI [1])
Informed Consent
Item
patients with written consent by their own volition after being provided sufficient explanation for the participation into this clinical trial
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Statins | Fibrates
Item
patients taking statins or fibrates
boolean
C0360714 (UMLS CUI [1])
C1449704 (UMLS CUI [2])
Study Subject Participation Status | Medical contraindication pitavastatin
Item
patients enrolled to the other trials using contraindication drugs of pitavastatin
boolean
C2348568 (UMLS CUI [1])
C1301624 (UMLS CUI [2,1])
C1101838 (UMLS CUI [2,2])
Myocardial Infarction
Item
patients who had acute myocardial infarction within six months before the day of the agreement acquisition
boolean
C0027051 (UMLS CUI [1])
Percutaneous Coronary Intervention Scheduled | Coronary Artery Bypass Surgery Scheduled
Item
patients scheduled pci and cabg within six months after the day of the agreement acquisition
boolean
C1532338 (UMLS CUI [1,1])
C0205539 (UMLS CUI [1,2])
C0010055 (UMLS CUI [2,1])
C0205539 (UMLS CUI [2,2])
Malignant Neoplasms | Malignant Neoplasms Unlikely
Item
patients who had diagnosis or doubt of malignant tumor
boolean
C0006826 (UMLS CUI [1])
C0006826 (UMLS CUI [2,1])
C0750558 (UMLS CUI [2,2])
Medical contraindication pitavastatin
Item
patients corresponded to "contraindications" of pitavastatin
boolean
C1301624 (UMLS CUI [1,1])
C1101838 (UMLS CUI [1,2])
Hypercholesterolemia, Familial
Item
familial hypercholesterolemia patients
boolean
C0020445 (UMLS CUI [1])
Patients Ineligible
Item
patients judged ineligible by investigators
boolean
C0030705 (UMLS CUI [1,1])
C1512714 (UMLS CUI [1,2])