ID

20017

Beschrijving

Defining The Role Of Dialysate Magnesium In Arrhythmogenicity On Dialysis; ODM derived from: https://clinicaltrials.gov/show/NCT00242164

Link

https://clinicaltrials.gov/show/NCT00242164

Trefwoorden

Versies (1)
  1. 03-02-17 03-02-17 -
Geüploaded op

3 februari 2017

DOI

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Licentie

Creative Commons BY 4.0
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Eligibility Chronic Kidney Disease NCT00242164

Engels

Eligibility Chronic Kidney Disease NCT00242164

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
18 years of age and over with end-stage renal disease. (esrd)
Beschrijving

Age | Kidney Failure, Chronic

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
UMLS CUI [2]
C0022661
have been on maintenance hemodialysis therapy three times/week for greater than or equal to 3 months
Beschrijving

Maintenance hemodialysis Frequency Duration

Datatype

boolean

Alias
UMLS CUI [1,1]
C4040576
UMLS CUI [1,2]
C0376249
UMLS CUI [1,3]
C0449238
all causes of renal failure are included
Beschrijving

Kidney Failure Causes All

Datatype

boolean

Alias
UMLS CUI [1,1]
C0035078
UMLS CUI [1,2]
C0015127
UMLS CUI [1,3]
C0444868
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
less than 18 years of age
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
have been on maintenance hemodialysis therapy three times/week for less than 3 months
Beschrijving

Maintenance hemodialysis Frequency Duration

Datatype

boolean

Alias
UMLS CUI [1,1]
C4040576
UMLS CUI [1,2]
C0376249
UMLS CUI [1,3]
C0449238
are pregnant or lactating
Beschrijving

Pregnancy | Breast Feeding

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
unable or unwilling to provide informed consent
Beschrijving

Informed Consent Unable | Informed Consent Unwilling

Datatype

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1299582
UMLS CUI [2,1]
C0021430
UMLS CUI [2,2]
C0558080
currently participating in a clinical trial with an intervention
Beschrijving

Study Subject Participation Status | Clinical Trial Intervention

Datatype

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2,1]
C0008976
UMLS CUI [2,2]
C0184661
systolic (top number) blood pressure levels greater than or equal to 180 or less then 80
Beschrijving

Systolic Pressure

Datatype

boolean

Alias
UMLS CUI [1]
C0871470
diastolic (bottom number) blood pressure levels greater than 110
Beschrijving

Diastolic blood pressure

Datatype

boolean

Alias
UMLS CUI [1]
C0428883
a hemoglobin level (red blood cell measure) that is less than 8mg/dl
Beschrijving

Hemoglobin measurement | Red Blood Cell Count measurement

Datatype

boolean

Alias
UMLS CUI [1]
C0518015
UMLS CUI [2]
C0014772
a corrected calcium level that is greater than 11mg/dl or less than 8mg/dl
Beschrijving

Corrected serum calcium measurement

Datatype

boolean

Alias
UMLS CUI [1]
C0455288
had a change in their anti-hypertensive medications within the last three weeks
Beschrijving

Antihypertensive Agents Change

Datatype

boolean

Alias
UMLS CUI [1,1]
C0003364
UMLS CUI [1,2]
C0392747
clinical signs and symptoms of untreated or unresolved infection
Beschrijving

Signs and Symptoms Clinical | Communicable Disease untreated | Communicable Disease Resolution Lacking

Datatype

boolean

Alias
UMLS CUI [1,1]
C0037088
UMLS CUI [1,2]
C0205210
UMLS CUI [2,1]
C0009450
UMLS CUI [2,2]
C0332155
UMLS CUI [3,1]
C0009450
UMLS CUI [3,2]
C1514893
UMLS CUI [3,3]
C0332268
clinical evidence requiring admission to the hospital
Beschrijving

Hospital admission Requirement Evidence Clinical

Datatype

boolean

Alias
UMLS CUI [1,1]
C0184666
UMLS CUI [1,2]
C1514873
UMLS CUI [1,3]
C3887511
UMLS CUI [1,4]
C0205210
had a cerebral vascular accident or myocardial incident within the past 3 months
Beschrijving

Cerebrovascular accident | Incident Myocardial

Datatype

boolean

Alias
UMLS CUI [1]
C0038454
UMLS CUI [2,1]
C1551358
UMLS CUI [2,2]
C1522564
based on the assessment of the investigators, or study coordinator designee, patients who appear unlikely or unable to participate in the required study procedures
Beschrijving

Protocol Compliance Unlikely | Protocol Compliance Unable

Datatype

boolean

Alias
UMLS CUI [1,1]
C0525058
UMLS CUI [1,2]
C0750558
UMLS CUI [2,1]
C0525058
UMLS CUI [2,2]
C1299582
patients with a history of arrhythmias, recent electrophysiological evaluation and or having pacemakers are excluded.
Beschrijving

Cardiac Arrhythmia | electrophysiological study | Artificial cardiac pacemaker

Datatype

boolean

Alias
UMLS CUI [1]
C0003811
UMLS CUI [2]
C0850293
UMLS CUI [3]
C0030163
patients with acute renal failure.
Beschrijving

Kidney Failure

Datatype

boolean

Alias
UMLS CUI [1]
C0035078
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Similar models

Eligibility Chronic Kidney Disease NCT00242164

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Age | Kidney Failure, Chronic
Item
18 years of age and over with end-stage renal disease. (esrd)
boolean
C0001779 (UMLS CUI [1])
C0022661 (UMLS CUI [2])
Maintenance hemodialysis Frequency Duration
Item
have been on maintenance hemodialysis therapy three times/week for greater than or equal to 3 months
boolean
C4040576 (UMLS CUI [1,1])
C0376249 (UMLS CUI [1,2])
C0449238 (UMLS CUI [1,3])
Kidney Failure Causes All
Item
all causes of renal failure are included
boolean
C0035078 (UMLS CUI [1,1])
C0015127 (UMLS CUI [1,2])
C0444868 (UMLS CUI [1,3])
Item Group
C0680251 (UMLS CUI)
Age
Item
less than 18 years of age
boolean
C0001779 (UMLS CUI [1])
Maintenance hemodialysis Frequency Duration
Item
have been on maintenance hemodialysis therapy three times/week for less than 3 months
boolean
C4040576 (UMLS CUI [1,1])
C0376249 (UMLS CUI [1,2])
C0449238 (UMLS CUI [1,3])
Pregnancy | Breast Feeding
Item
are pregnant or lactating
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Informed Consent Unable | Informed Consent Unwilling
Item
unable or unwilling to provide informed consent
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2,1])
C0558080 (UMLS CUI [2,2])
Study Subject Participation Status | Clinical Trial Intervention
Item
currently participating in a clinical trial with an intervention
boolean
C2348568 (UMLS CUI [1])
C0008976 (UMLS CUI [2,1])
C0184661 (UMLS CUI [2,2])
Systolic Pressure
Item
systolic (top number) blood pressure levels greater than or equal to 180 or less then 80
boolean
C0871470 (UMLS CUI [1])
Diastolic blood pressure
Item
diastolic (bottom number) blood pressure levels greater than 110
boolean
C0428883 (UMLS CUI [1])
Hemoglobin measurement | Red Blood Cell Count measurement
Item
a hemoglobin level (red blood cell measure) that is less than 8mg/dl
boolean
C0518015 (UMLS CUI [1])
C0014772 (UMLS CUI [2])
Corrected serum calcium measurement
Item
a corrected calcium level that is greater than 11mg/dl or less than 8mg/dl
boolean
C0455288 (UMLS CUI [1])
Antihypertensive Agents Change
Item
had a change in their anti-hypertensive medications within the last three weeks
boolean
C0003364 (UMLS CUI [1,1])
C0392747 (UMLS CUI [1,2])
Signs and Symptoms Clinical | Communicable Disease untreated | Communicable Disease Resolution Lacking
Item
clinical signs and symptoms of untreated or unresolved infection
boolean
C0037088 (UMLS CUI [1,1])
C0205210 (UMLS CUI [1,2])
C0009450 (UMLS CUI [2,1])
C0332155 (UMLS CUI [2,2])
C0009450 (UMLS CUI [3,1])
C1514893 (UMLS CUI [3,2])
C0332268 (UMLS CUI [3,3])
Hospital admission Requirement Evidence Clinical
Item
clinical evidence requiring admission to the hospital
boolean
C0184666 (UMLS CUI [1,1])
C1514873 (UMLS CUI [1,2])
C3887511 (UMLS CUI [1,3])
C0205210 (UMLS CUI [1,4])
Cerebrovascular accident | Incident Myocardial
Item
had a cerebral vascular accident or myocardial incident within the past 3 months
boolean
C0038454 (UMLS CUI [1])
C1551358 (UMLS CUI [2,1])
C1522564 (UMLS CUI [2,2])
Protocol Compliance Unlikely | Protocol Compliance Unable
Item
based on the assessment of the investigators, or study coordinator designee, patients who appear unlikely or unable to participate in the required study procedures
boolean
C0525058 (UMLS CUI [1,1])
C0750558 (UMLS CUI [1,2])
C0525058 (UMLS CUI [2,1])
C1299582 (UMLS CUI [2,2])
Cardiac Arrhythmia | electrophysiological study | Artificial cardiac pacemaker
Item
patients with a history of arrhythmias, recent electrophysiological evaluation and or having pacemakers are excluded.
boolean
C0003811 (UMLS CUI [1])
C0850293 (UMLS CUI [2])
C0030163 (UMLS CUI [3])
Kidney Failure
Item
patients with acute renal failure.
boolean
C0035078 (UMLS CUI [1])
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