ID

35628

Beschrijving

Prevalence of Chronic Kidney Disease and Its Association With Clinical Outcome in Patients With Coronary Heart Disease; ODM derived from: https://clinicaltrials.gov/show/NCT02509013

Link

https://clinicaltrials.gov/show/NCT02509013

Trefwoorden

Versies (1)
  1. 12-03-19 12-03-19 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

12 maart 2019

DOI

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Licentie

Creative Commons BY 4.0
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Eligibility Coronary Heart Disease NCT02509013

Engels

Eligibility Coronary Heart Disease NCT02509013

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
age≥18 years.
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
patients with clinical evidence of stable coronary heart disease, who meet at least one of the following three criterias:
Beschrijving

Coronary heart disease Stable | Criteria Fulfill

Datatype

boolean

Alias
UMLS CUI [1,1]
C0010068
UMLS CUI [1,2]
C0205360
UMLS CUI [2,1]
C0243161
UMLS CUI [2,2]
C1550543
a. stable coronary heart disease with objective evidence of atherosclerosis, either coronary angiography shows ≥50% stenosis of at least one of the coronary main stems or first-level branches, or typical exertional angina pectoris with positive stress tests(ecg stress test, echocardiograph stress test, or stress radionuclide myocardial imaging). b diagnosed of myocardial infarction at least 3 months before recruitment. c.coronary revascularization(pci or cabg) at least 3 months before recruitment.
Beschrijving

Coronary heart disease Stable | Atherosclerosis | Coronary angiography | Stenosis Percentage Left coronary artery main stem | Stenosis Percentage Branch of Coronary artery | Exercise-induced angina | Stress Test Positive | Exercise stress ECG test | Echocardiography findings during stress test | Exercise stress test Myocardial imaging | Myocardial Infarction | Coronary revascularisation | Percutaneous Coronary Intervention | Coronary Artery Bypass Surgery

Datatype

boolean

Alias
UMLS CUI [1,1]
C0010068
UMLS CUI [1,2]
C0205360
UMLS CUI [2]
C0004153
UMLS CUI [3]
C0085532
UMLS CUI [4,1]
C1261287
UMLS CUI [4,2]
C0439165
UMLS CUI [4,3]
C0226031
UMLS CUI [5,1]
C1261287
UMLS CUI [5,2]
C0439165
UMLS CUI [5,3]
C1253959
UMLS CUI [5,4]
C0205042
UMLS CUI [6]
C0577698
UMLS CUI [7,1]
C3494508
UMLS CUI [7,2]
C1514241
UMLS CUI [8]
C1304755
UMLS CUI [9]
C2040901
UMLS CUI [10,1]
C0015260
UMLS CUI [10,2]
C0203713
UMLS CUI [11]
C0027051
UMLS CUI [12]
C0877341
UMLS CUI [13]
C1532338
UMLS CUI [14]
C0010055
informed consent signed by patients or legal guardians.
Beschrijving

Informed Consent | Informed Consent Guardian

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
UMLS CUI [2,1]
C0021430
UMLS CUI [2,2]
C1274041
willing to and capable of being followed up for 1 year.
Beschrijving

Follow-up Willing | Follow-up Able

Datatype

boolean

Alias
UMLS CUI [1,1]
C3274571
UMLS CUI [1,2]
C0600109
UMLS CUI [2,1]
C3274571
UMLS CUI [2,2]
C1299581
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
non-atherosclerotic coronary heart disease
Beschrijving

Coronary heart disease | Exception Atherosclerosis

Datatype

boolean

Alias
UMLS CUI [1]
C0010068
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C0004153
deterioration of heart failure during the past 3 months
Beschrijving

Heart failure Deterioration

Datatype

boolean

Alias
UMLS CUI [1,1]
C0018801
UMLS CUI [1,2]
C0868945
exposed to contrast agent during the past one month.
Beschrijving

Exposure to Contrast Media

Datatype

boolean

Alias
UMLS CUI [1,1]
C0332157
UMLS CUI [1,2]
C0009924
history of amputation
Beschrijving

Amputation

Datatype

boolean

Alias
UMLS CUI [1]
C0002688
pregnancy
Beschrijving

Pregnancy

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
female patients in menstrual period(still eligible after menstrual period)
Beschrijving

Gender Menstrual cycle

Datatype

boolean

Alias
UMLS CUI [1,1]
C0079399
UMLS CUI [1,2]
C0025329
organ failure other than heart failure and kidney failure
Beschrijving

Organ failure | Exception Heart failure | Exception Kidney Failure

Datatype

boolean

Alias
UMLS CUI [1]
C0349410
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C0018801
UMLS CUI [3,1]
C1705847
UMLS CUI [3,2]
C0035078
comorbid other diseases, and life expectancy <1 year
Beschrijving

Comorbidity | Life Expectancy

Datatype

boolean

Alias
UMLS CUI [1]
C0009488
UMLS CUI [2]
C0023671
considered not fit for the study due to other reasons, including but not restricted to : a. severe infection; b. acute kidney injury.
Beschrijving

Patient Medically unfit Clinical Trial | Communicable Disease Severe | Injury of kidney

Datatype

boolean

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C3841806
UMLS CUI [1,3]
C0008976
UMLS CUI [2,1]
C0009450
UMLS CUI [2,2]
C0205082
UMLS CUI [3]
C0160420
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Similar models

Eligibility Coronary Heart Disease NCT02509013

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
age≥18 years.
boolean
C0001779 (UMLS CUI [1])
Coronary heart disease Stable | Criteria Fulfill
Item
patients with clinical evidence of stable coronary heart disease, who meet at least one of the following three criterias:
boolean
C0010068 (UMLS CUI [1,1])
C0205360 (UMLS CUI [1,2])
C0243161 (UMLS CUI [2,1])
C1550543 (UMLS CUI [2,2])
Coronary heart disease Stable | Atherosclerosis | Coronary angiography | Stenosis Percentage Left coronary artery main stem | Stenosis Percentage Branch of Coronary artery | Exercise-induced angina | Stress Test Positive | Exercise stress ECG test | Echocardiography findings during stress test | Exercise stress test Myocardial imaging | Myocardial Infarction | Coronary revascularisation | Percutaneous Coronary Intervention | Coronary Artery Bypass Surgery
Item
a. stable coronary heart disease with objective evidence of atherosclerosis, either coronary angiography shows ≥50% stenosis of at least one of the coronary main stems or first-level branches, or typical exertional angina pectoris with positive stress tests(ecg stress test, echocardiograph stress test, or stress radionuclide myocardial imaging). b diagnosed of myocardial infarction at least 3 months before recruitment. c.coronary revascularization(pci or cabg) at least 3 months before recruitment.
boolean
C0010068 (UMLS CUI [1,1])
C0205360 (UMLS CUI [1,2])
C0004153 (UMLS CUI [2])
C0085532 (UMLS CUI [3])
C1261287 (UMLS CUI [4,1])
C0439165 (UMLS CUI [4,2])
C0226031 (UMLS CUI [4,3])
C1261287 (UMLS CUI [5,1])
C0439165 (UMLS CUI [5,2])
C1253959 (UMLS CUI [5,3])
C0205042 (UMLS CUI [5,4])
C0577698 (UMLS CUI [6])
C3494508 (UMLS CUI [7,1])
C1514241 (UMLS CUI [7,2])
C1304755 (UMLS CUI [8])
C2040901 (UMLS CUI [9])
C0015260 (UMLS CUI [10,1])
C0203713 (UMLS CUI [10,2])
C0027051 (UMLS CUI [11])
C0877341 (UMLS CUI [12])
C1532338 (UMLS CUI [13])
C0010055 (UMLS CUI [14])
Informed Consent | Informed Consent Guardian
Item
informed consent signed by patients or legal guardians.
boolean
C0021430 (UMLS CUI [1])
C0021430 (UMLS CUI [2,1])
C1274041 (UMLS CUI [2,2])
Follow-up Willing | Follow-up Able
Item
willing to and capable of being followed up for 1 year.
boolean
C3274571 (UMLS CUI [1,1])
C0600109 (UMLS CUI [1,2])
C3274571 (UMLS CUI [2,1])
C1299581 (UMLS CUI [2,2])
Item Group
C0680251 (UMLS CUI)
Coronary heart disease | Exception Atherosclerosis
Item
non-atherosclerotic coronary heart disease
boolean
C0010068 (UMLS CUI [1])
C1705847 (UMLS CUI [2,1])
C0004153 (UMLS CUI [2,2])
Heart failure Deterioration
Item
deterioration of heart failure during the past 3 months
boolean
C0018801 (UMLS CUI [1,1])
C0868945 (UMLS CUI [1,2])
Exposure to Contrast Media
Item
exposed to contrast agent during the past one month.
boolean
C0332157 (UMLS CUI [1,1])
C0009924 (UMLS CUI [1,2])
Amputation
Item
history of amputation
boolean
C0002688 (UMLS CUI [1])
Pregnancy
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])
Gender Menstrual cycle
Item
female patients in menstrual period(still eligible after menstrual period)
boolean
C0079399 (UMLS CUI [1,1])
C0025329 (UMLS CUI [1,2])
Organ failure | Exception Heart failure | Exception Kidney Failure
Item
organ failure other than heart failure and kidney failure
boolean
C0349410 (UMLS CUI [1])
C1705847 (UMLS CUI [2,1])
C0018801 (UMLS CUI [2,2])
C1705847 (UMLS CUI [3,1])
C0035078 (UMLS CUI [3,2])
Comorbidity | Life Expectancy
Item
comorbid other diseases, and life expectancy <1 year
boolean
C0009488 (UMLS CUI [1])
C0023671 (UMLS CUI [2])
Patient Medically unfit Clinical Trial | Communicable Disease Severe | Injury of kidney
Item
considered not fit for the study due to other reasons, including but not restricted to : a. severe infection; b. acute kidney injury.
boolean
C0030705 (UMLS CUI [1,1])
C3841806 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
C0009450 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
C0160420 (UMLS CUI [3])
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