ID

29444

Beschrijving

A Quality Ensuring Project With Focus On Patients With Cardiovascular Diseases As Well As Type 2 Diabetes.; ODM derived from: https://clinicaltrials.gov/show/NCT00415428

Link

https://clinicaltrials.gov/show/NCT00415428

Trefwoorden

Versies (1)
  1. 25-03-18 25-03-18 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

25 maart 2018

DOI

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Creative Commons BY 4.0
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Eligibility Heart Diseases NCT00415428

Engels

Eligibility Heart Diseases NCT00415428

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
subjects had to meet all of the inclusion criteria to be eligible for enrollment into the study. the following subjects qualify for inclusion in the study:
Beschrijving

Criteria Fulfill

Datatype

boolean

Alias
UMLS CUI [1,1]
C0243161
UMLS CUI [1,2]
C1550543
subjects for whom measurement of total cholesterol, low density lipoprotein (ldl) cholesterol, blood pressure (bp) and glycosylated hemoglobin (hba1c) was planned independently of this observational study and for whom baseline values were or became available.
Beschrijving

Serum total cholesterol measurement | Low density lipoprotein cholesterol measurement | Blood pressure determination | Hemoglobin A1c measurement

Datatype

boolean

Alias
UMLS CUI [1]
C1445957
UMLS CUI [2]
C0202117
UMLS CUI [3]
C0005824
UMLS CUI [4]
C0474680
subjects with known cvd diagnosed > or = 6 months before inclusion
Beschrijving

Cardiovascular Diseases

Datatype

boolean

Alias
UMLS CUI [1]
C0007222
previous myocardial infarction
Beschrijving

Myocardial Infarction

Datatype

boolean

Alias
UMLS CUI [1]
C0027051
ischemic heart disease (stable and unstable angina pectoris)
Beschrijving

Myocardial Ischemia | Stable angina | Angina, Unstable

Datatype

boolean

Alias
UMLS CUI [1]
C0151744
UMLS CUI [2]
C0340288
UMLS CUI [3]
C0002965
ischemic apoplexy
Beschrijving

Ischemic stroke

Datatype

boolean

Alias
UMLS CUI [1]
C0948008
peripheral arterial disease
Beschrijving

Peripheral Arterial Diseases

Datatype

boolean

Alias
UMLS CUI [1]
C1704436
and/or
Beschrijving

ID.8

Datatype

boolean

subjects with t2d diagnosed > or = 6 months before inclusion
Beschrijving

Diabetes Mellitus, Non-Insulin-Dependent

Datatype

boolean

Alias
UMLS CUI [1]
C0011860
at least 50% of the subjects had to have cvd as the primary diagnosis. it was allowed for a secondary diagnosis to be <6 months before inclusion.
Beschrijving

Cardiovascular Disease Principal diagnosis Percent Minimum | Cardiovascular Disease Secondary diagnosis allowed

Datatype

boolean

Alias
UMLS CUI [1,1]
C0007222
UMLS CUI [1,2]
C0332137
UMLS CUI [1,3]
C0439165
UMLS CUI [1,4]
C1524031
UMLS CUI [2,1]
C0007222
UMLS CUI [2,2]
C0332138
UMLS CUI [2,3]
C0683607
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
subjects presenting with any of the following were not to be included in the study:
Beschrijving

Criteria Fulfill

Datatype

boolean

Alias
UMLS CUI [1,1]
C0243161
UMLS CUI [1,2]
C1550543
life expectancy of < or = 2 years
Beschrijving

Life Expectancy

Datatype

boolean

Alias
UMLS CUI [1]
C0023671
unable/unwilling to understand/follow instructions
Beschrijving

Compliance behavior Unable | Compliance behavior Unwilling

Datatype

boolean

Alias
UMLS CUI [1,1]
C1321605
UMLS CUI [1,2]
C1299582
UMLS CUI [2,1]
C1321605
UMLS CUI [2,2]
C0558080
taking part in a clinical study involving an investigational drug
Beschrijving

Study Subject Participation Status | Investigational New Drugs

Datatype

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2]
C0013230
followed by a specialist for their cvd and/or t2d at the time of inclusion in the study
Beschrijving

Follow-up Specialist Cardiovascular Diseases | Follow-up Specialist Non-Insulin-Dependent Diabetes Mellitus

Datatype

boolean

Alias
UMLS CUI [1,1]
C1522577
UMLS CUI [1,2]
C2348234
UMLS CUI [1,3]
C0007222
UMLS CUI [2,1]
C1522577
UMLS CUI [2,2]
C2348234
UMLS CUI [2,3]
C0011860
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Similar models

Eligibility Heart Diseases NCT00415428

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Criteria Fulfill
Item
subjects had to meet all of the inclusion criteria to be eligible for enrollment into the study. the following subjects qualify for inclusion in the study:
boolean
C0243161 (UMLS CUI [1,1])
C1550543 (UMLS CUI [1,2])
Serum total cholesterol measurement | Low density lipoprotein cholesterol measurement | Blood pressure determination | Hemoglobin A1c measurement
Item
subjects for whom measurement of total cholesterol, low density lipoprotein (ldl) cholesterol, blood pressure (bp) and glycosylated hemoglobin (hba1c) was planned independently of this observational study and for whom baseline values were or became available.
boolean
C1445957 (UMLS CUI [1])
C0202117 (UMLS CUI [2])
C0005824 (UMLS CUI [3])
C0474680 (UMLS CUI [4])
Cardiovascular Diseases
Item
subjects with known cvd diagnosed > or = 6 months before inclusion
boolean
C0007222 (UMLS CUI [1])
Myocardial Infarction
Item
previous myocardial infarction
boolean
C0027051 (UMLS CUI [1])
Myocardial Ischemia | Stable angina | Angina, Unstable
Item
ischemic heart disease (stable and unstable angina pectoris)
boolean
C0151744 (UMLS CUI [1])
C0340288 (UMLS CUI [2])
C0002965 (UMLS CUI [3])
Ischemic stroke
Item
ischemic apoplexy
boolean
C0948008 (UMLS CUI [1])
Peripheral Arterial Diseases
Item
peripheral arterial disease
boolean
C1704436 (UMLS CUI [1])
ID.8
Item
and/or
boolean
Diabetes Mellitus, Non-Insulin-Dependent
Item
subjects with t2d diagnosed > or = 6 months before inclusion
boolean
C0011860 (UMLS CUI [1])
Cardiovascular Disease Principal diagnosis Percent Minimum | Cardiovascular Disease Secondary diagnosis allowed
Item
at least 50% of the subjects had to have cvd as the primary diagnosis. it was allowed for a secondary diagnosis to be <6 months before inclusion.
boolean
C0007222 (UMLS CUI [1,1])
C0332137 (UMLS CUI [1,2])
C0439165 (UMLS CUI [1,3])
C1524031 (UMLS CUI [1,4])
C0007222 (UMLS CUI [2,1])
C0332138 (UMLS CUI [2,2])
C0683607 (UMLS CUI [2,3])
Item Group
C0680251 (UMLS CUI)
Criteria Fulfill
Item
subjects presenting with any of the following were not to be included in the study:
boolean
C0243161 (UMLS CUI [1,1])
C1550543 (UMLS CUI [1,2])
Life Expectancy
Item
life expectancy of < or = 2 years
boolean
C0023671 (UMLS CUI [1])
Compliance behavior Unable | Compliance behavior Unwilling
Item
unable/unwilling to understand/follow instructions
boolean
C1321605 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C1321605 (UMLS CUI [2,1])
C0558080 (UMLS CUI [2,2])
Study Subject Participation Status | Investigational New Drugs
Item
taking part in a clinical study involving an investigational drug
boolean
C2348568 (UMLS CUI [1])
C0013230 (UMLS CUI [2])
Follow-up Specialist Cardiovascular Diseases | Follow-up Specialist Non-Insulin-Dependent Diabetes Mellitus
Item
followed by a specialist for their cvd and/or t2d at the time of inclusion in the study
boolean
C1522577 (UMLS CUI [1,1])
C2348234 (UMLS CUI [1,2])
C0007222 (UMLS CUI [1,3])
C1522577 (UMLS CUI [2,1])
C2348234 (UMLS CUI [2,2])
C0011860 (UMLS CUI [2,3])
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