ID

35300

Beschrijving

The optImal Hydration With sodiuM chloridE in High Risk Patients Undergoing Coronary Angiography; ODM derived from: https://clinicaltrials.gov/show/NCT02232997

Link

https://clinicaltrials.gov/show/NCT02232997

Trefwoorden

  1. 26-02-19 26-02-19 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

26 februari 2019

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Chronic Kidney Disease NCT02232997

Eligibility Chronic Kidney Disease NCT02232997

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients undergoing coronary angiography;
Beschrijving

Coronary angiography

Datatype

boolean

Alias
UMLS CUI [1]
C0085532
an estimated glomerular filtration rate (egfr) of 60 ml/min per 1·73 m2 or lower;
Beschrijving

Estimated Glomerular Filtration Rate

Datatype

boolean

Alias
UMLS CUI [1]
C3811844
age 18 years or older;
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
at least one of the following: diabetes mellitus, history of congestive heart failure, hypertension (blood pressure >140/90 mm hg or treatment with anti-
Beschrijving

Diabetes Mellitus | Congestive heart failure | Hypertensive disease | Blood pressure determination

Datatype

boolean

Alias
UMLS CUI [1]
C0011849
UMLS CUI [2]
C0018802
UMLS CUI [3]
C0020538
UMLS CUI [4]
C0005824
hypertensive medication), or age older than 75 years.
Beschrijving

Antihypertensive Agents | Age

Datatype

boolean

Alias
UMLS CUI [1]
C0003364
UMLS CUI [2]
C0001779
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
inability to obtain consent from participants;
Beschrijving

Informed Consent Unable

Datatype

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1299582
emergency cardiac catheterisation (eg, primary percutaneous coronary intervention for st-segment elevation myocardial infarction);
Beschrijving

Emergency Cardiac Catheterization | Percutaneous Coronary Intervention Primary ST segment elevation myocardial infarction

Datatype

boolean

Alias
UMLS CUI [1,1]
C0013956
UMLS CUI [1,2]
C0018795
UMLS CUI [2,1]
C1532338
UMLS CUI [2,2]
C0205225
UMLS CUI [2,3]
C1536220
renal replacement therapy;
Beschrijving

Renal Replacement Therapy

Datatype

boolean

Alias
UMLS CUI [1]
C0206074
exposure to radiographic contrast media within the previous 2 days and in the future 3 days;
Beschrijving

Exposure to Radiographic contrast media

Datatype

boolean

Alias
UMLS CUI [1,1]
C0332157
UMLS CUI [1,2]
C2930749
allergy to radiographic contrast media;
Beschrijving

Allergy to X-ray contrast media

Datatype

boolean

Alias
UMLS CUI [1]
C0570563
acute decompensated heart failure;
Beschrijving

Decompensated cardiac failure

Datatype

boolean

Alias
UMLS CUI [1]
C0581377
severe valvular heart disease;
Beschrijving

Heart valve disease Severe

Datatype

boolean

Alias
UMLS CUI [1,1]
C0018824
UMLS CUI [1,2]
C0205082
left ventricular thrombus;
Beschrijving

Left ventricular thrombus

Datatype

boolean

Alias
UMLS CUI [1]
C0587044
history of kidney or heart transplantation;
Beschrijving

Kidney Transplantation | Heart Transplantation

Datatype

boolean

Alias
UMLS CUI [1]
C0022671
UMLS CUI [2]
C0018823
change in estimated gfr of 7.5% or more per day or a cumulative change of 15% or more during the preceding 2 or more days(two blood samples collected within 3 months).
Beschrijving

Estimated Glomerular Filtration Rate Change Percentage Timespan | Blood specimen Quantity

Datatype

boolean

Alias
UMLS CUI [1,1]
C3811844
UMLS CUI [1,2]
C0443172
UMLS CUI [1,3]
C0439165
UMLS CUI [1,4]
C0872291
UMLS CUI [2,1]
C0178913
UMLS CUI [2,2]
C1265611

Similar models

Eligibility Chronic Kidney Disease NCT02232997

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Coronary angiography
Item
patients undergoing coronary angiography;
boolean
C0085532 (UMLS CUI [1])
Estimated Glomerular Filtration Rate
Item
an estimated glomerular filtration rate (egfr) of 60 ml/min per 1·73 m2 or lower;
boolean
C3811844 (UMLS CUI [1])
Age
Item
age 18 years or older;
boolean
C0001779 (UMLS CUI [1])
Diabetes Mellitus | Congestive heart failure | Hypertensive disease | Blood pressure determination
Item
at least one of the following: diabetes mellitus, history of congestive heart failure, hypertension (blood pressure >140/90 mm hg or treatment with anti-
boolean
C0011849 (UMLS CUI [1])
C0018802 (UMLS CUI [2])
C0020538 (UMLS CUI [3])
C0005824 (UMLS CUI [4])
Antihypertensive Agents | Age
Item
hypertensive medication), or age older than 75 years.
boolean
C0003364 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
Informed Consent Unable
Item
inability to obtain consent from participants;
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
Emergency Cardiac Catheterization | Percutaneous Coronary Intervention Primary ST segment elevation myocardial infarction
Item
emergency cardiac catheterisation (eg, primary percutaneous coronary intervention for st-segment elevation myocardial infarction);
boolean
C0013956 (UMLS CUI [1,1])
C0018795 (UMLS CUI [1,2])
C1532338 (UMLS CUI [2,1])
C0205225 (UMLS CUI [2,2])
C1536220 (UMLS CUI [2,3])
Renal Replacement Therapy
Item
renal replacement therapy;
boolean
C0206074 (UMLS CUI [1])
Exposure to Radiographic contrast media
Item
exposure to radiographic contrast media within the previous 2 days and in the future 3 days;
boolean
C0332157 (UMLS CUI [1,1])
C2930749 (UMLS CUI [1,2])
Allergy to X-ray contrast media
Item
allergy to radiographic contrast media;
boolean
C0570563 (UMLS CUI [1])
Decompensated cardiac failure
Item
acute decompensated heart failure;
boolean
C0581377 (UMLS CUI [1])
Heart valve disease Severe
Item
severe valvular heart disease;
boolean
C0018824 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
Left ventricular thrombus
Item
left ventricular thrombus;
boolean
C0587044 (UMLS CUI [1])
Kidney Transplantation | Heart Transplantation
Item
history of kidney or heart transplantation;
boolean
C0022671 (UMLS CUI [1])
C0018823 (UMLS CUI [2])
Estimated Glomerular Filtration Rate Change Percentage Timespan | Blood specimen Quantity
Item
change in estimated gfr of 7.5% or more per day or a cumulative change of 15% or more during the preceding 2 or more days(two blood samples collected within 3 months).
boolean
C3811844 (UMLS CUI [1,1])
C0443172 (UMLS CUI [1,2])
C0439165 (UMLS CUI [1,3])
C0872291 (UMLS CUI [1,4])
C0178913 (UMLS CUI [2,1])
C1265611 (UMLS CUI [2,2])

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