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Eligibility

1 forms  
  1. StudyEvent: Eligibility
    1. Eligibility
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI 2011AA
CL425202
age 18 Years to 65 Years
Description

age 18 Years to 65 Years

Data type

boolean

Alias
UMLS CUI 2011AA
C0001779
SNOMED CT 2011_0131
397669002
Dilated cardiomyopathy
Description

Dilated cardiomyopathy

Data type

boolean

Alias
UMLS CUI 2011AA
C0007193
SNOMED CT 2011_0131
195021004
MedDRA 14.1
10056419
ICD-10-CM Version 2010
I42.0
UMLS CUI 2011AA
C0011900
SNOMED CT 2011_0131
439401001
LOINC Version 232
MTHU008876
LVEF <= 40% determined by contrast echocardiography
Description

LVEF <= 40% determined by contrast echocardiography

Data type

boolean

Alias
UMLS CUI 2011AA
C0428772
SNOMED CT 2011_0131
250908004
MedDRA 14.1
10069170
UMLS CUI 2011AA
C0521095
SNOMED CT 2011_0131
436000
UMLS CUI 2011AA
C0013518
SNOMED CT 2011_0131
433231002
NYHA class II - IV
Description

NYHA class II - IV

Data type

boolean

Alias
UMLS CUI 2011AA
C1319794
SNOMED CT 2011_0131
421704003
MedDRA 14.1
10064080
UMLS CUI 2011AA
C1319795
SNOMED CT 2011_0131
420913000
MedDRA 14.1
10064081
UMLS CUI 2011AA
C1319796
SNOMED CT 2011_0131
422293003
MedDRA 14.1
10064082
Age 18 - 65
Description

Age 18 - 65

Data type

boolean

Alias
UMLS CUI 2011AA
C0001779
SNOMED CT 2011_0131
397669002
Disease duration: symptomatic heart failure >1 year and <5 years prior to screening date
Description

Disease duration: symptomatic heart failure >1 year and <5 years prior to screening date

Data type

boolean

Alias
UMLS CUI 2011AA
C0872146
UMLS CUI 2011AA
C0231220
SNOMED CT 2011_0131
264931009
UMLS CUI 2011AA
C0018801
SNOMED CT 2011_0131
155374007
MedDRA 14.1
10019279
ICD-9-CM Version 2011
428
CTCAE 1105E
E10124
UMLS CUI 2011AA
C0439234
SNOMED CT 2011_0131
258707000
HL7 V3 2006_05
Y
UMLS CUI 2011AA
C0332152
SNOMED CT 2011_0131
288556008
UMLS CUI 2011AA
C1409616
UMLS CUI 2011AA
C0011008
SNOMED CT 2011_0131
410671006
LOINC Version 232
MTHU021546
Treatment with ACE inhibitors or angiotensin II receptor blockers (ARB), beta-blockers, and aldosterone antagonists (the latter at the discretion of the attending physician), for at least 6 months and at stable doses for at least 2 months prior to screening date.
Description

Treatment with ACE inhibitors or angiotensin II receptor blockers (ARB), beta-blockers, and aldosterone antagonists (the latter at the discretion of the attending physician), for at least 6 months and at stable doses for at least 2 months prior to screening date.

Data type

boolean

Alias
UMLS CUI 2011AA
C0039798
UMLS CUI 2011AA
C0003015
SNOMED CT 2011_0131
372733002
UMLS CUI 2011AA
C0521942
SNOMED CT 2011_0131
372913009
UMLS CUI 2011AA
C0001645
SNOMED CT 2011_0131
33252009
LOINC Version 232
MTHU003324
UMLS CUI 2011AA
C0002007
SNOMED CT 2011_0131
372603003
UMLS CUI 2011AA
C1320929
SNOMED CT 2011_0131
405279007
HL7 V3 2006_05
ATTPHYS
UMLS CUI 2011AA
C0439231
SNOMED CT 2011_0131
258706009
HL7 V3 2006_05
MO
UMLS CUI 2011AA
C0205360
SNOMED CT 2011_0131
58158008
LOINC Version 232
MTHU015276
UMLS CUI 2011AA
C0178602
SNOMED CT 2011_0131
260911001
UMLS CUI 2011AA
C0332152
SNOMED CT 2011_0131
288556008
UMLS CUI 2011AA
C1409616
UMLS CUI 2011AA
C0011008
SNOMED CT 2011_0131
410671006
LOINC Version 232
MTHU021546
Informed Consent
Description

The patient's informed consent

Data type

boolean

Alias
UMLS CUI 2011AA
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI 2011AA
CL425201
NYHA class IV patients who are bed-ridden and dependent upon parenteral medication
Description

NYHA class IV patients who are bed-ridden and dependent upon parenteral medication

Data type

boolean

Alias
UMLS CUI 2011AA
C1319796
SNOMED CT 2011_0131
422293003
MedDRA 14.1
10064082
UMLS CUI 2011AA
C0425251
SNOMED CT 2011_0131
160685001
LOINC Version 232
MTHU008262
UMLS CUI 2011AA
CL414916
UMLS CUI 2011AA
C1518896
UMLS CUI 2011AA
C0013227
Cardiac insufficiency resulting from another basic disease (e.g. coronary artery disease, >= 50% stenosis of major vessel as ascertained by coronary angiography performed more recent than three years before screening date, hypertensive heart disease, or valvular defects >second degree
Description

Cardiac insufficiency resulting from another basic disease (e.g. coronary artery disease, >= 50% stenosis of major vessel as ascertained by coronary angiography performed more recent than three years before screening date, hypertensive heart disease, or valvular defects >second degree

Data type

boolean

Alias
UMLS CUI 2011AA
C0018801
SNOMED CT 2011_0131
155374007
MedDRA 14.1
10019279
ICD-9-CM Version 2011
428
CTCAE 1105E
E10124
UMLS CUI 2011AA
C1274040
SNOMED CT 2011_0131
79409006
UMLS CUI 2011AA
C0205394
SNOMED CT 2011_0131
74964007
UMLS CUI 2011AA
C0012634
SNOMED CT 2011_0131
64572001
UMLS CUI 2011AA
C0010068
SNOMED CT 2011_0131
53741008
MedDRA 14.1
10068617
UMLS CUI 2011AA
C0679403
MedDRA 14.1
10057469
UMLS CUI 2011AA
C0085532
SNOMED CT 2011_0131
33367005
MedDRA 14.1
10003200
UMLS CUI 2011AA
C0439234
SNOMED CT 2011_0131
258707000
HL7 V3 2006_05
Y
UMLS CUI 2011AA
C0332152
SNOMED CT 2011_0131
288556008
UMLS CUI 2011AA
C1409616
UMLS CUI 2011AA
C0011008
SNOMED CT 2011_0131
410671006
LOINC Version 232
MTHU021546
UMLS CUI 2011AA
C0152105
SNOMED CT 2011_0131
64715009
MedDRA 14.1
10020823
ICD-10-CM Version 2010
I11
ICD-9-CM Version 2011
402
UMLS CUI 2011AA
C2748945
UMLS CUI 2011AA
C0449286
SNOMED CT 2011_0131
246173007
History of - myocardial infarction
Description

History of myocardial infarction

Data type

boolean

Alias
UMLS CUI 2011AA
C1275835
SNOMED CT 2011_0131
399211009
Acute myocarditis according to Dallas criteria
Description

Acute myocarditis according to Dallas criteria

Data type

boolean

Alias
UMLS CUI 2011AA
C0155686
SNOMED CT 2011_0131
46701001
MedDRA 14.1
10000932
ICD-10-CM Version 2010
I40.9
ICD-9-CM Version 2011
422.90
UMLS CUI 2011AA
C1706462
UMLS CUI 2011AA
C0679228
Endocrine disorder excluding insulin-dependent diabetes mellitus
Description

Endocrine disorder excluding insulin-dependent diabetes mellitus

Data type

boolean

Alias
UMLS CUI 2011AA
C0014130
SNOMED CT 2011_0131
362969004
MedDRA 14.1
10014695
LOINC Version 232
MTHU021570
ICD-10-CM Version 2010
E34.9
ICD-9-CM Version 2011
259.9
UMLS CUI 2011AA
CL411789
UMLS CUI 2011AA
C0011854
SNOMED CT 2011_0131
46635009
MedDRA 14.1
10067584
LOINC Version 232
MTHU020217
ICD-10-CM Version 2010
E10
Implanted cardiac defibrillator (ICD) <1 month before screening date
Description

Implanted cardiac defibrillator (ICD) <1 month before screening date

Data type

boolean

Alias
UMLS CUI 2011AA
C0021102
SNOMED CT 2011_0131
40388003
UMLS CUI 2011AA
CL383027
UMLS CUI 2011AA
C0439231
SNOMED CT 2011_0131
258706009
HL7 V3 2006_05
MO
UMLS CUI 2011AA
C0332152
SNOMED CT 2011_0131
288556008
UMLS CUI 2011AA
C1409616
UMLS CUI 2011AA
C0011008
SNOMED CT 2011_0131
410671006
LOINC Version 232
MTHU021546
Cardiac resynchronization therapy (CRT) <6 months before screening date
Description

Cardiac resynchronization therapy (CRT) <6 months before screening date

Data type

boolean

Alias
UMLS CUI 2011AA
C1167956
MedDRA 14.1
10059862
UMLS CUI 2011AA
C0439231
SNOMED CT 2011_0131
258706009
HL7 V3 2006_05
MO
UMLS CUI 2011AA
C0332152
SNOMED CT 2011_0131
288556008
UMLS CUI 2011AA
C1409616
UMLS CUI 2011AA
C0011008
SNOMED CT 2011_0131
410671006
LOINC Version 232
MTHU021546
I.v. medication with inotropic drugs, vasodilators or repeated (>1/day) i.v. administration of diuretics.
Description

I.v. medication with inotropic drugs, vasodilators or repeated (>1/day) i.v. administration of diuretics.

Data type

boolean

Alias
UMLS CUI 2011AA
C0348016
SNOMED CT 2011_0131
255560000
UMLS CUI 2011AA
C0013227
UMLS CUI 2011AA
C0304509
SNOMED CT 2011_0131
111139005
UMLS CUI 2011AA
C0042402
SNOMED CT 2011_0131
58944007
UMLS CUI 2011AA
C0205341
SNOMED CT 2011_0131
27582007
UMLS CUI 2011AA
C0013125
UMLS CUI 2011AA
C0439228
SNOMED CT 2011_0131
258703001
HL7 V3 2006_05
D
UMLS CUI 2011AA
C0012798
SNOMED CT 2011_0131
372695000
LOINC Version 232
MTHU003217
Active infectious disease, or signs of ongoing infection with CRP >10mmol/L
Description

Active infectious disease, or signs of ongoing infection with CRP >10mmol/L

Data type

boolean

Alias
UMLS CUI 2011AA
C0205177
SNOMED CT 2011_0131
55561003
UMLS CUI 2011AA
C0009450
SNOMED CT 2011_0131
40733004
MedDRA 14.1
10021881
LOINC Version 232
MTHU034915
ICD-9-CM Version 2011
136.9
UMLS CUI 2011AA
C0220912
UMLS CUI 2011AA
C0750536
UMLS CUI 2011AA
C0021311
SNOMED CT 2011_0131
257551009
MedDRA 14.1
10021789
UMLS CUI 2011AA
C0006560
SNOMED CT 2011_0131
61425002
LOINC Version 232
MTHU002335
Impaired renal function (serum creatinine >220 µmol/L)
Description

Impaired renal function (serum creatinine >220 µmol/L)

Data type

boolean

Alias
UMLS CUI 2011AA
C0341697
Any disease requiring immunosuppressive drugs
Description

Any disease requiring immunosuppressive drugs

Data type

boolean

Alias
UMLS CUI 2011AA
C0012634
SNOMED CT 2011_0131
64572001
UMLS CUI 2011AA
C1514873
UMLS CUI 2011AA
C0021081
SNOMED CT 2011_0131
372823004, 69431002
Anaemia (haemoglobin below 90 g/L) due to other causes than CHF
Description

Anaemia (haemoglobin below 90 g/L) due to other causes than CHF

Data type

boolean

Alias
UMLS CUI 2011AA
C0002871
SNOMED CT 2011_0131
271737000
MedDRA 14.1
10002034
LOINC Version 232
MTHU020823
ICD-10-CM Version 2010
D64.9
ICD-9-CM Version 2011
285.9
CTCAE 1105E
E10010
UMLS CUI 2011AA
C0019046
SNOMED CT 2011_0131
38082009
MedDRA 14.1
10019481
LOINC Version 232
LP14449-0
UMLS CUI 2011AA
CL384716
UMLS CUI 2011AA
C1314792
SNOMED CT 2011_0131
134198009
UMLS CUI 2011AA
CL411789
UMLS CUI 2011AA
C0018802
SNOMED CT 2011_0131
42343007
MedDRA 14.1
10007559
LOINC Version 232
MTHU020787
ICD-10-CM Version 2010
I50.9
ICD-9-CM Version 2011
428.0
Pregnancy or lactation, or childbearing potential without appropriate contraception
Description

Pregnancy or lactation, or childbearing potential without appropriate contraception

Data type

boolean

Alias
UMLS CUI 2011AA
C0549206
UMLS CUI 2011AA
C0006147
Alcohol or drug abuse
Description

Alcohol or drug abuse

Data type

boolean

Alias
UMLS CUI 2011AA
C0237123
Presence of a malignant tumour, or remission of malignancy < 5 years
Description

Presence of a malignant tumour, or remission of malignancy < 5 years

Data type

boolean

Alias
UMLS CUI 2011AA
C0006826
SNOMED CT 2011_0131
363346000
MedDRA 14.1
10028997
LOINC Version 232
MTHU010328
ICD-10-CM Version 2010
C00-C96
UMLS CUI 2011AA
C0150312
SNOMED CT 2011_0131
52101004
UMLS CUI 2011AA
C0544452
SNOMED CT 2011_0131
277022003
UMLS CUI 2011AA
C0439234
SNOMED CT 2011_0131
258707000
HL7 V3 2006_05
Y
Suspected poor capability to follow instructions and cooperate
Description

Suspected poor capability to follow instructions and cooperate

Data type

boolean

Alias
UMLS CUI 2011AA
C0750491
SNOMED CT 2011_0131
415684004
UMLS CUI 2011AA
C0205169
SNOMED CT 2011_0131
556001
UMLS CUI 2011AA
C2698977
SNOMED CT 2011_0131
415684004
UMLS CUI 2011AA
C0302828
UMLS CUI 2011AA
C1321605
SNOMED CT 2011_0131
405078008
UMLS CUI 2011AA
C0424350
SNOMED CT 2011_0131
248042003
Another life-threatening disease with poor prognosis (survival < 2 years)
Description

Another life-threatening disease with poor prognosis (survival < 2 years)

Data type

boolean

Alias
UMLS CUI 2011AA
C0205394
SNOMED CT 2011_0131
74964007
UMLS CUI 2011AA
C1610642
SNOMED CT 2011_0131
440181000
UMLS CUI 2011AA
C0278252
SNOMED CT 2011_0131
170969009
UMLS CUI 2011AA
C0220921
UMLS CUI 2011AA
C0439234
SNOMED CT 2011_0131
258707000
HL7 V3 2006_05
Y
Participation in any other clinical study within < 30 days prior to screening date
Description

Participation in any other clinical study within < 30 days prior to screening date

Data type

boolean

Alias
UMLS CUI 2011AA
C0679823
HL7 V3 2006_05
PART
UMLS CUI 2011AA
C0205394
SNOMED CT 2011_0131
74964007
UMLS CUI 2011AA
C0008976
SNOMED CT 2011_0131
110465008
UMLS CUI 2011AA
C0439228
SNOMED CT 2011_0131
258703001
HL7 V3 2006_05
D
UMLS CUI 2011AA
C0332152
SNOMED CT 2011_0131
288556008
UMLS CUI 2011AA
C1409616
UMLS CUI 2011AA
C0011008
SNOMED CT 2011_0131
410671006
LOINC Version 232
MTHU021546
Previous treatments with IA or immunoglobulin
Description

Previous treatments with IA or immunoglobulin

Data type

boolean

Alias
UMLS CUI 2011AA
C1514463
UMLS CUI 2011AA
C0301904
SNOMED CT 2011_0131
33066005
UMLS CUI 2011AA
C0021027
SNOMED CT 2011_0131
399771004
HL7 V3 2006_05
14
Contraindications for application of echocardiography contrast agent (Luminity(R) according to Luminity(R) specifications, including cardiac shunts, pulmonary vascular compromise)
Description

Contraindications for application of echocardiography contrast agent (Luminity(R) according to Luminity(R) specifications, including cardiac shunts, pulmonary vascular compromise)

Data type

boolean

Alias
UMLS CUI 2011AA
C1301624
SNOMED CT 2011_0131
397745006
UMLS CUI 2011AA
CL025718
UMLS CUI 2011AA
C0013518
SNOMED CT 2011_0131
433231002
UMLS CUI 2011AA
C1254351
UMLS CUI 2011AA
C0937858
SNOMED CT 2011_0131
409292001
UMLS CUI 2011AA
C2348235
LOINC Version 232
MTHU032336
UMLS CUI 2011AA
C0332257
SNOMED CT 2011_0131
55919000
UMLS CUI 2011AA
C0232180
SNOMED CT 2011_0131
442119001
UMLS CUI 2011AA
C0854416
MedDRA 14.1
10061474
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Similar models

Eligibility

1 forms
  1. StudyEvent: Eligibility
    1. Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Inclusion Criteria
CL425202 (UMLS CUI 2011AA)
age 18 Years to 65 Years
Item
age 18 Years to 65 Years
boolean
C0001779 (UMLS CUI 2011AA)
397669002 (SNOMED CT 2011_0131)
Dilated cardiomyopathy
Item
Dilated cardiomyopathy
boolean
C0007193 (UMLS CUI 2011AA)
195021004 (SNOMED CT 2011_0131)
10056419 (MedDRA 14.1)
I42.0 (ICD-10-CM Version 2010)
C0011900 (UMLS CUI 2011AA)
439401001 (SNOMED CT 2011_0131)
MTHU008876 (LOINC Version 232)
LVEF <= 40% determined by contrast echocardiography
Item
LVEF <= 40% determined by contrast echocardiography
boolean
C0428772 (UMLS CUI 2011AA)
250908004 (SNOMED CT 2011_0131)
10069170 (MedDRA 14.1)
C0521095 (UMLS CUI 2011AA)
436000 (SNOMED CT 2011_0131)
C0013518 (UMLS CUI 2011AA)
433231002 (SNOMED CT 2011_0131)
NYHA class II - IV
Item
NYHA class II - IV
boolean
C1319794 (UMLS CUI 2011AA)
421704003 (SNOMED CT 2011_0131)
10064080 (MedDRA 14.1)
C1319795 (UMLS CUI 2011AA)
420913000 (SNOMED CT 2011_0131)
10064081 (MedDRA 14.1)
C1319796 (UMLS CUI 2011AA)
422293003 (SNOMED CT 2011_0131)
10064082 (MedDRA 14.1)
Age 18 - 65
Item
Age 18 - 65
boolean
C0001779 (UMLS CUI 2011AA)
397669002 (SNOMED CT 2011_0131)
Disease duration: symptomatic heart failure >1 year and <5 years prior to screening date
Item
Disease duration: symptomatic heart failure >1 year and <5 years prior to screening date
boolean
C0872146 (UMLS CUI 2011AA)
C0231220 (UMLS CUI 2011AA)
264931009 (SNOMED CT 2011_0131)
C0018801 (UMLS CUI 2011AA)
155374007 (SNOMED CT 2011_0131)
10019279 (MedDRA 14.1)
428 (ICD-9-CM Version 2011)
E10124 (CTCAE 1105E)
C0439234 (UMLS CUI 2011AA)
258707000 (SNOMED CT 2011_0131)
Y (HL7 V3 2006_05)
C0332152 (UMLS CUI 2011AA)
288556008 (SNOMED CT 2011_0131)
C1409616 (UMLS CUI 2011AA)
C0011008 (UMLS CUI 2011AA)
410671006 (SNOMED CT 2011_0131)
MTHU021546 (LOINC Version 232)
Treatment with ACE inhibitors or angiotensin II receptor blockers (ARB), beta-blockers, and aldosterone antagonists (the latter at the discretion of the attending physician), for at least 6 months and at stable doses for at least 2 months prior to screening date.
Item
Treatment with ACE inhibitors or angiotensin II receptor blockers (ARB), beta-blockers, and aldosterone antagonists (the latter at the discretion of the attending physician), for at least 6 months and at stable doses for at least 2 months prior to screening date.
boolean
C0039798 (UMLS CUI 2011AA)
C0003015 (UMLS CUI 2011AA)
372733002 (SNOMED CT 2011_0131)
C0521942 (UMLS CUI 2011AA)
372913009 (SNOMED CT 2011_0131)
C0001645 (UMLS CUI 2011AA)
33252009 (SNOMED CT 2011_0131)
MTHU003324 (LOINC Version 232)
C0002007 (UMLS CUI 2011AA)
372603003 (SNOMED CT 2011_0131)
C1320929 (UMLS CUI 2011AA)
405279007 (SNOMED CT 2011_0131)
ATTPHYS (HL7 V3 2006_05)
C0439231 (UMLS CUI 2011AA)
258706009 (SNOMED CT 2011_0131)
MO (HL7 V3 2006_05)
C0205360 (UMLS CUI 2011AA)
58158008 (SNOMED CT 2011_0131)
MTHU015276 (LOINC Version 232)
C0178602 (UMLS CUI 2011AA)
260911001 (SNOMED CT 2011_0131)
C0332152 (UMLS CUI 2011AA)
288556008 (SNOMED CT 2011_0131)
C1409616 (UMLS CUI 2011AA)
C0011008 (UMLS CUI 2011AA)
410671006 (SNOMED CT 2011_0131)
MTHU021546 (LOINC Version 232)
The patient's informed consent
Item
Informed Consent
boolean
C0021430 (UMLS CUI 2011AA)
Item Group
Exclusion Criteria
CL425201 (UMLS CUI 2011AA)
NYHA class IV patients who are bed-ridden and dependent upon parenteral medication
Item
NYHA class IV patients who are bed-ridden and dependent upon parenteral medication
boolean
C1319796 (UMLS CUI 2011AA)
422293003 (SNOMED CT 2011_0131)
10064082 (MedDRA 14.1)
C0425251 (UMLS CUI 2011AA)
160685001 (SNOMED CT 2011_0131)
MTHU008262 (LOINC Version 232)
CL414916 (UMLS CUI 2011AA)
C1518896 (UMLS CUI 2011AA)
C0013227 (UMLS CUI 2011AA)
Cardiac insufficiency resulting from another basic disease (e.g. coronary artery disease, >= 50% stenosis of major vessel as ascertained by coronary angiography performed more recent than three years before screening date, hypertensive heart disease, or valvular defects >second degree
Item
Cardiac insufficiency resulting from another basic disease (e.g. coronary artery disease, >= 50% stenosis of major vessel as ascertained by coronary angiography performed more recent than three years before screening date, hypertensive heart disease, or valvular defects >second degree
boolean
C0018801 (UMLS CUI 2011AA)
155374007 (SNOMED CT 2011_0131)
10019279 (MedDRA 14.1)
428 (ICD-9-CM Version 2011)
E10124 (CTCAE 1105E)
C1274040 (UMLS CUI 2011AA)
79409006 (SNOMED CT 2011_0131)
C0205394 (UMLS CUI 2011AA)
74964007 (SNOMED CT 2011_0131)
C0012634 (UMLS CUI 2011AA)
64572001 (SNOMED CT 2011_0131)
C0010068 (UMLS CUI 2011AA)
53741008 (SNOMED CT 2011_0131)
10068617 (MedDRA 14.1)
C0679403 (UMLS CUI 2011AA)
10057469 (MedDRA 14.1)
C0085532 (UMLS CUI 2011AA)
33367005 (SNOMED CT 2011_0131)
10003200 (MedDRA 14.1)
C0439234 (UMLS CUI 2011AA)
258707000 (SNOMED CT 2011_0131)
Y (HL7 V3 2006_05)
C0332152 (UMLS CUI 2011AA)
288556008 (SNOMED CT 2011_0131)
C1409616 (UMLS CUI 2011AA)
C0011008 (UMLS CUI 2011AA)
410671006 (SNOMED CT 2011_0131)
MTHU021546 (LOINC Version 232)
C0152105 (UMLS CUI 2011AA)
64715009 (SNOMED CT 2011_0131)
10020823 (MedDRA 14.1)
I11 (ICD-10-CM Version 2010)
402 (ICD-9-CM Version 2011)
C2748945 (UMLS CUI 2011AA)
C0449286 (UMLS CUI 2011AA)
246173007 (SNOMED CT 2011_0131)
History of myocardial infarction
Item
History of - myocardial infarction
boolean
C1275835 (UMLS CUI 2011AA)
399211009 (SNOMED CT 2011_0131)
Acute myocarditis according to Dallas criteria
Item
Acute myocarditis according to Dallas criteria
boolean
C0155686 (UMLS CUI 2011AA)
46701001 (SNOMED CT 2011_0131)
10000932 (MedDRA 14.1)
I40.9 (ICD-10-CM Version 2010)
422.90 (ICD-9-CM Version 2011)
C1706462 (UMLS CUI 2011AA)
C0679228 (UMLS CUI 2011AA)
Endocrine disorder excluding insulin-dependent diabetes mellitus
Item
Endocrine disorder excluding insulin-dependent diabetes mellitus
boolean
C0014130 (UMLS CUI 2011AA)
362969004 (SNOMED CT 2011_0131)
10014695 (MedDRA 14.1)
MTHU021570 (LOINC Version 232)
E34.9 (ICD-10-CM Version 2010)
259.9 (ICD-9-CM Version 2011)
CL411789 (UMLS CUI 2011AA)
C0011854 (UMLS CUI 2011AA)
46635009 (SNOMED CT 2011_0131)
10067584 (MedDRA 14.1)
MTHU020217 (LOINC Version 232)
E10 (ICD-10-CM Version 2010)
Implanted cardiac defibrillator (ICD) <1 month before screening date
Item
Implanted cardiac defibrillator (ICD) <1 month before screening date
boolean
C0021102 (UMLS CUI 2011AA)
40388003 (SNOMED CT 2011_0131)
CL383027 (UMLS CUI 2011AA)
C0439231 (UMLS CUI 2011AA)
258706009 (SNOMED CT 2011_0131)
MO (HL7 V3 2006_05)
C0332152 (UMLS CUI 2011AA)
288556008 (SNOMED CT 2011_0131)
C1409616 (UMLS CUI 2011AA)
C0011008 (UMLS CUI 2011AA)
410671006 (SNOMED CT 2011_0131)
MTHU021546 (LOINC Version 232)
Cardiac resynchronization therapy (CRT) <6 months before screening date
Item
Cardiac resynchronization therapy (CRT) <6 months before screening date
boolean
C1167956 (UMLS CUI 2011AA)
10059862 (MedDRA 14.1)
C0439231 (UMLS CUI 2011AA)
258706009 (SNOMED CT 2011_0131)
MO (HL7 V3 2006_05)
C0332152 (UMLS CUI 2011AA)
288556008 (SNOMED CT 2011_0131)
C1409616 (UMLS CUI 2011AA)
C0011008 (UMLS CUI 2011AA)
410671006 (SNOMED CT 2011_0131)
MTHU021546 (LOINC Version 232)
I.v. medication with inotropic drugs, vasodilators or repeated (>1/day) i.v. administration of diuretics.
Item
I.v. medication with inotropic drugs, vasodilators or repeated (>1/day) i.v. administration of diuretics.
boolean
C0348016 (UMLS CUI 2011AA)
255560000 (SNOMED CT 2011_0131)
C0013227 (UMLS CUI 2011AA)
C0304509 (UMLS CUI 2011AA)
111139005 (SNOMED CT 2011_0131)
C0042402 (UMLS CUI 2011AA)
58944007 (SNOMED CT 2011_0131)
C0205341 (UMLS CUI 2011AA)
27582007 (SNOMED CT 2011_0131)
C0013125 (UMLS CUI 2011AA)
C0439228 (UMLS CUI 2011AA)
258703001 (SNOMED CT 2011_0131)
D (HL7 V3 2006_05)
C0012798 (UMLS CUI 2011AA)
372695000 (SNOMED CT 2011_0131)
MTHU003217 (LOINC Version 232)
Active infectious disease, or signs of ongoing infection with CRP >10mmol/L
Item
Active infectious disease, or signs of ongoing infection with CRP >10mmol/L
boolean
C0205177 (UMLS CUI 2011AA)
55561003 (SNOMED CT 2011_0131)
C0009450 (UMLS CUI 2011AA)
40733004 (SNOMED CT 2011_0131)
10021881 (MedDRA 14.1)
MTHU034915 (LOINC Version 232)
136.9 (ICD-9-CM Version 2011)
C0220912 (UMLS CUI 2011AA)
C0750536 (UMLS CUI 2011AA)
C0021311 (UMLS CUI 2011AA)
257551009 (SNOMED CT 2011_0131)
10021789 (MedDRA 14.1)
C0006560 (UMLS CUI 2011AA)
61425002 (SNOMED CT 2011_0131)
MTHU002335 (LOINC Version 232)
Impaired renal function (serum creatinine >220 µmol/L)
Item
Impaired renal function (serum creatinine >220 µmol/L)
boolean
C0341697 (UMLS CUI 2011AA)
Any disease requiring immunosuppressive drugs
Item
Any disease requiring immunosuppressive drugs
boolean
C0012634 (UMLS CUI 2011AA)
64572001 (SNOMED CT 2011_0131)
C1514873 (UMLS CUI 2011AA)
C0021081 (UMLS CUI 2011AA)
372823004, 69431002 (SNOMED CT 2011_0131)
Anaemia (haemoglobin below 90 g/L) due to other causes than CHF
Item
Anaemia (haemoglobin below 90 g/L) due to other causes than CHF
boolean
C0002871 (UMLS CUI 2011AA)
271737000 (SNOMED CT 2011_0131)
10002034 (MedDRA 14.1)
MTHU020823 (LOINC Version 232)
D64.9 (ICD-10-CM Version 2010)
285.9 (ICD-9-CM Version 2011)
E10010 (CTCAE 1105E)
C0019046 (UMLS CUI 2011AA)
38082009 (SNOMED CT 2011_0131)
10019481 (MedDRA 14.1)
LP14449-0 (LOINC Version 232)
CL384716 (UMLS CUI 2011AA)
C1314792 (UMLS CUI 2011AA)
134198009 (SNOMED CT 2011_0131)
CL411789 (UMLS CUI 2011AA)
C0018802 (UMLS CUI 2011AA)
42343007 (SNOMED CT 2011_0131)
10007559 (MedDRA 14.1)
MTHU020787 (LOINC Version 232)
I50.9 (ICD-10-CM Version 2010)
428.0 (ICD-9-CM Version 2011)
Pregnancy or lactation, or childbearing potential without appropriate contraception
Item
Pregnancy or lactation, or childbearing potential without appropriate contraception
boolean
C0549206 (UMLS CUI 2011AA)
C0006147 (UMLS CUI 2011AA)
Alcohol or drug abuse
Item
Alcohol or drug abuse
boolean
C0237123 (UMLS CUI 2011AA)
Presence of a malignant tumour, or remission of malignancy < 5 years
Item
Presence of a malignant tumour, or remission of malignancy < 5 years
boolean
C0006826 (UMLS CUI 2011AA)
363346000 (SNOMED CT 2011_0131)
10028997 (MedDRA 14.1)
MTHU010328 (LOINC Version 232)
C00-C96 (ICD-10-CM Version 2010)
C0150312 (UMLS CUI 2011AA)
52101004 (SNOMED CT 2011_0131)
C0544452 (UMLS CUI 2011AA)
277022003 (SNOMED CT 2011_0131)
C0439234 (UMLS CUI 2011AA)
258707000 (SNOMED CT 2011_0131)
Y (HL7 V3 2006_05)
Suspected poor capability to follow instructions and cooperate
Item
Suspected poor capability to follow instructions and cooperate
boolean
C0750491 (UMLS CUI 2011AA)
415684004 (SNOMED CT 2011_0131)
C0205169 (UMLS CUI 2011AA)
556001 (SNOMED CT 2011_0131)
C2698977 (UMLS CUI 2011AA)
415684004 (SNOMED CT 2011_0131)
C0302828 (UMLS CUI 2011AA)
C1321605 (UMLS CUI 2011AA)
405078008 (SNOMED CT 2011_0131)
C0424350 (UMLS CUI 2011AA)
248042003 (SNOMED CT 2011_0131)
Another life-threatening disease with poor prognosis (survival < 2 years)
Item
Another life-threatening disease with poor prognosis (survival < 2 years)
boolean
C0205394 (UMLS CUI 2011AA)
74964007 (SNOMED CT 2011_0131)
C1610642 (UMLS CUI 2011AA)
440181000 (SNOMED CT 2011_0131)
C0278252 (UMLS CUI 2011AA)
170969009 (SNOMED CT 2011_0131)
C0220921 (UMLS CUI 2011AA)
C0439234 (UMLS CUI 2011AA)
258707000 (SNOMED CT 2011_0131)
Y (HL7 V3 2006_05)
Participation in any other clinical study within < 30 days prior to screening date
Item
Participation in any other clinical study within < 30 days prior to screening date
boolean
C0679823 (UMLS CUI 2011AA)
PART (HL7 V3 2006_05)
C0205394 (UMLS CUI 2011AA)
74964007 (SNOMED CT 2011_0131)
C0008976 (UMLS CUI 2011AA)
110465008 (SNOMED CT 2011_0131)
C0439228 (UMLS CUI 2011AA)
258703001 (SNOMED CT 2011_0131)
D (HL7 V3 2006_05)
C0332152 (UMLS CUI 2011AA)
288556008 (SNOMED CT 2011_0131)
C1409616 (UMLS CUI 2011AA)
C0011008 (UMLS CUI 2011AA)
410671006 (SNOMED CT 2011_0131)
MTHU021546 (LOINC Version 232)
Previous treatments with IA or immunoglobulin
Item
Previous treatments with IA or immunoglobulin
boolean
C1514463 (UMLS CUI 2011AA)
C0301904 (UMLS CUI 2011AA)
33066005 (SNOMED CT 2011_0131)
C0021027 (UMLS CUI 2011AA)
399771004 (SNOMED CT 2011_0131)
14 (HL7 V3 2006_05)
Contraindications for application of echocardiography contrast agent (Luminity(R) according to Luminity(R) specifications, including cardiac shunts, pulmonary vascular compromise)
Item
Contraindications for application of echocardiography contrast agent (Luminity(R) according to Luminity(R) specifications, including cardiac shunts, pulmonary vascular compromise)
boolean
C1301624 (UMLS CUI 2011AA)
397745006 (SNOMED CT 2011_0131)
CL025718 (UMLS CUI 2011AA)
C0013518 (UMLS CUI 2011AA)
433231002 (SNOMED CT 2011_0131)
C1254351 (UMLS CUI 2011AA)
C0937858 (UMLS CUI 2011AA)
409292001 (SNOMED CT 2011_0131)
C2348235 (UMLS CUI 2011AA)
MTHU032336 (LOINC Version 232)
C0332257 (UMLS CUI 2011AA)
55919000 (SNOMED CT 2011_0131)
C0232180 (UMLS CUI 2011AA)
442119001 (SNOMED CT 2011_0131)
C0854416 (UMLS CUI 2011AA)
10061474 (MedDRA 14.1)
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