ID

35098

Beschrijving

Computed Tomography and Biomarker Analysis in Diagnosing Coronary Artery Disease in Asymptomatic Patients Who Have Undergone Stem Cell Transplant; ODM derived from: https://clinicaltrials.gov/show/NCT02077218

Link

https://clinicaltrials.gov/show/NCT02077218

Trefwoorden

Versies (2)
  1. 16-02-19 16-02-19 -
  2. 16-02-19 16-02-19 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

16 februari 2019

DOI

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Licentie

Creative Commons BY 4.0
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Eligibility Cancer Survivor NCT02077218

Engels

Eligibility Cancer Survivor NCT02077218

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
alive and in complete remission at time of enrollment
Beschrijving

Alive | In complete remission

Datatype

boolean

Alias
UMLS CUI [1]
C2584946
UMLS CUI [2]
C0677874
underwent allogeneic hct after 1995
Beschrijving

Allogeneic Hematopoietic Stem Cell Transplantation

Datatype

boolean

Alias
UMLS CUI [1]
C1705576
time between hct and study entry: >= 2 years
Beschrijving

Allogeneic Hematopoietic Stem Cell Transplantation Time Interval Enrollment in clinical trial

Datatype

boolean

Alias
UMLS CUI [1,1]
C1705576
UMLS CUI [1,2]
C0872291
UMLS CUI [1,3]
C4041024
have at least one cvrf (hypertension, diabetes, dyslipidemia) at the time of eligibility determination
Beschrijving

Cardiovascular risk factors Quantity | Hypertensive disease | Diabetes Mellitus | Dyslipidemia

Datatype

boolean

Alias
UMLS CUI [1,1]
C0850624
UMLS CUI [1,2]
C1265611
UMLS CUI [2]
C0020538
UMLS CUI [3]
C0011849
UMLS CUI [4]
C0242339
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
history of ischemic heart disease, stroke, or cardiomyopathy/congestive heart failure
Beschrijving

Myocardial Ischemia | Cerebrovascular accident | Cardiomyopathy | Congestive heart failure

Datatype

boolean

Alias
UMLS CUI [1]
C0151744
UMLS CUI [2]
C0038454
UMLS CUI [3]
C0878544
UMLS CUI [4]
C0018802
abnormal renal function (glomerular filtration rate [gfr] < 60 ml/min/1.73m2)
Beschrijving

Abnormal renal function | Glomerular Filtration Rate

Datatype

boolean

Alias
UMLS CUI [1]
C0151746
UMLS CUI [2]
C0017654
pregnancy
Beschrijving

Pregnancy

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
known allergy to intravenous (iv) contrast
Beschrijving

Allergy to intravenous contrast media

Datatype

boolean

Alias
UMLS CUI [1]
C2242530
sustained or symptomatic ventricular dysrhythmias uncontrolled with drug therapy or implantable device; significant conduction defects (i.e.: second or third degree atrioventricular block or sick sinus syndrome)
Beschrijving

Ventricular arrhythmia Sustained | Ventricular arrhythmia Symptomatic | Pharmacotherapy Lacking | Implanted device Lacking | Conduction defects | Second degree atrioventricular block | Complete atrioventricular block | Sick Sinus Syndrome

Datatype

boolean

Alias
UMLS CUI [1,1]
C0085612
UMLS CUI [1,2]
C0443318
UMLS CUI [2,1]
C0085612
UMLS CUI [2,2]
C0231220
UMLS CUI [3,1]
C0013216
UMLS CUI [3,2]
C0332268
UMLS CUI [4,1]
C0021102
UMLS CUI [4,2]
C0332268
UMLS CUI [5]
C0264886
UMLS CUI [6]
C0264906
UMLS CUI [7]
C0151517
UMLS CUI [8]
C0037052
current clinical evidence of moderate-to-severe obstructive pulmonary disease or reactive airway diseases (i.e.: asthma) requiring therapy
Beschrijving

Obstructive Lung Disease Moderate | Obstructive Lung Disease Severe | Reactive airway disease Treatment required for | Asthma

Datatype

boolean

Alias
UMLS CUI [1,1]
C0600260
UMLS CUI [1,2]
C0205081
UMLS CUI [2,1]
C0600260
UMLS CUI [2,2]
C0205082
UMLS CUI [3,1]
C3714497
UMLS CUI [3,2]
C0332121
UMLS CUI [4]
C0004096
history of drug sensitivity or allergic reaction to beta-blockers
Beschrijving

BETA BLOCKER ALLERGY

Datatype

boolean

Alias
UMLS CUI [1]
C0741466
currently taking calcium channel blockers such as verapramil and diltiazem
Beschrijving

Calcium Channel Blockers | Verapamil | Diltiazem

Datatype

boolean

Alias
UMLS CUI [1]
C0006684
UMLS CUI [2]
C0042523
UMLS CUI [3]
C0012373
history of unrepaired severe aortic stenosis
Beschrijving

Aortic stenosis, severe | Repair Lacking

Datatype

boolean

Alias
UMLS CUI [1]
C3806272
UMLS CUI [2,1]
C4319951
UMLS CUI [2,2]
C0332268
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Similar models

Eligibility Cancer Survivor NCT02077218

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Alive | In complete remission
Item
alive and in complete remission at time of enrollment
boolean
C2584946 (UMLS CUI [1])
C0677874 (UMLS CUI [2])
Allogeneic Hematopoietic Stem Cell Transplantation
Item
underwent allogeneic hct after 1995
boolean
C1705576 (UMLS CUI [1])
Allogeneic Hematopoietic Stem Cell Transplantation Time Interval Enrollment in clinical trial
Item
time between hct and study entry: >= 2 years
boolean
C1705576 (UMLS CUI [1,1])
C0872291 (UMLS CUI [1,2])
C4041024 (UMLS CUI [1,3])
Cardiovascular risk factors Quantity | Hypertensive disease | Diabetes Mellitus | Dyslipidemia
Item
have at least one cvrf (hypertension, diabetes, dyslipidemia) at the time of eligibility determination
boolean
C0850624 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C0020538 (UMLS CUI [2])
C0011849 (UMLS CUI [3])
C0242339 (UMLS CUI [4])
Item Group
C0680251 (UMLS CUI)
Myocardial Ischemia | Cerebrovascular accident | Cardiomyopathy | Congestive heart failure
Item
history of ischemic heart disease, stroke, or cardiomyopathy/congestive heart failure
boolean
C0151744 (UMLS CUI [1])
C0038454 (UMLS CUI [2])
C0878544 (UMLS CUI [3])
C0018802 (UMLS CUI [4])
Abnormal renal function | Glomerular Filtration Rate
Item
abnormal renal function (glomerular filtration rate [gfr] < 60 ml/min/1.73m2)
boolean
C0151746 (UMLS CUI [1])
C0017654 (UMLS CUI [2])
Pregnancy
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])
Allergy to intravenous contrast media
Item
known allergy to intravenous (iv) contrast
boolean
C2242530 (UMLS CUI [1])
Ventricular arrhythmia Sustained | Ventricular arrhythmia Symptomatic | Pharmacotherapy Lacking | Implanted device Lacking | Conduction defects | Second degree atrioventricular block | Complete atrioventricular block | Sick Sinus Syndrome
Item
sustained or symptomatic ventricular dysrhythmias uncontrolled with drug therapy or implantable device; significant conduction defects (i.e.: second or third degree atrioventricular block or sick sinus syndrome)
boolean
C0085612 (UMLS CUI [1,1])
C0443318 (UMLS CUI [1,2])
C0085612 (UMLS CUI [2,1])
C0231220 (UMLS CUI [2,2])
C0013216 (UMLS CUI [3,1])
C0332268 (UMLS CUI [3,2])
C0021102 (UMLS CUI [4,1])
C0332268 (UMLS CUI [4,2])
C0264886 (UMLS CUI [5])
C0264906 (UMLS CUI [6])
C0151517 (UMLS CUI [7])
C0037052 (UMLS CUI [8])
Obstructive Lung Disease Moderate | Obstructive Lung Disease Severe | Reactive airway disease Treatment required for | Asthma
Item
current clinical evidence of moderate-to-severe obstructive pulmonary disease or reactive airway diseases (i.e.: asthma) requiring therapy
boolean
C0600260 (UMLS CUI [1,1])
C0205081 (UMLS CUI [1,2])
C0600260 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
C3714497 (UMLS CUI [3,1])
C0332121 (UMLS CUI [3,2])
C0004096 (UMLS CUI [4])
BETA BLOCKER ALLERGY
Item
history of drug sensitivity or allergic reaction to beta-blockers
boolean
C0741466 (UMLS CUI [1])
Calcium Channel Blockers | Verapamil | Diltiazem
Item
currently taking calcium channel blockers such as verapramil and diltiazem
boolean
C0006684 (UMLS CUI [1])
C0042523 (UMLS CUI [2])
C0012373 (UMLS CUI [3])
Aortic stenosis, severe | Repair Lacking
Item
history of unrepaired severe aortic stenosis
boolean
C3806272 (UMLS CUI [1])
C4319951 (UMLS CUI [2,1])
C0332268 (UMLS CUI [2,2])
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