ID

27583

Beschrijving

Differential Intervention Trial by Standard Therapy Versus Pitavastatin in Patients With Chronic Hemodialysis (DIALYSIS); ODM derived from: https://clinicaltrials.gov/show/NCT00846118

Link

https://clinicaltrials.gov/show/NCT00846118

Trefwoorden

  1. 21-11-17 21-11-17 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

21 november 2017

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Cardiovascular Disease NCT00846118

Eligibility Cardiovascular Disease NCT00846118

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients under hemodialysis
Beschrijving

Hemodialysis

Datatype

boolean

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

Hypercholesterolemia

Datatype

boolean

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

Low density lipoprotein cholesterol measurement

Datatype

boolean

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

Serum total cholesterol measurement

Datatype

boolean

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

Anticholesteremic Agents Patient need for

Datatype

boolean

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

Age

Datatype

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
Beschrijving

Informed Consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients taking statins or fibrates
Beschrijving

Statins | Fibrates

Datatype

boolean

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

Study Subject Participation Status | Medical contraindication pitavastatin

Datatype

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
Beschrijving

Myocardial Infarction

Datatype

boolean

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

Percutaneous Coronary Intervention Scheduled | Coronary Artery Bypass Surgery Scheduled

Datatype

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
Beschrijving

Malignant Neoplasms | Malignant Neoplasms Unlikely

Datatype

boolean

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

Medical contraindication pitavastatin

Datatype

boolean

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

Hypercholesterolemia, Familial

Datatype

boolean

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

Patients Ineligible

Datatype

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)
Datatype
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])

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