Englisch

Eligibility Heart Failure NCT01354678

1 Formulare  
Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients with coronary artery disease (cad) and hf ii-iii nyha class
Beschreibung

Coronary Artery Disease | Heart failure New York Heart Association Classification

Datentyp

boolean

Alias
UMLS CUI [1]
C1956346
UMLS CUI [2,1]
C0018801
UMLS CUI [2,2]
C1275491
mi more than 6 months before the study
Beschreibung

Myocardial Infarction

Datentyp

boolean

Alias
UMLS CUI [1]
C0027051
lvef less than 35%
Beschreibung

Left ventricular ejection fraction

Datentyp

boolean

Alias
UMLS CUI [1]
C0428772
absence of indication to coronary revascularization
Beschreibung

Absence Indication Coronary revascularisation

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0332197
UMLS CUI [1,2]
C3146298
UMLS CUI [1,3]
C0877341
optimal pharmacological therapy no less than 8 weeks
Beschreibung

Pharmacotherapy Optimal

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0013216
UMLS CUI [1,2]
C2698651
heart transplantation is contraindicated
Beschreibung

Medical contraindication Heart Transplantation

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0018823
patients with implantable cardioverter-defibrillator (icd) or cardiac resynchronization therapy defibrillator (crt-d)
Beschreibung

Implantable defibrillator | Cardiac Resynchronization Therapy Devices

Datentyp

boolean

Alias
UMLS CUI [1]
C0162589
UMLS CUI [2]
C2936377
patients giving informed consent
Beschreibung

Informed Consent

Datentyp

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
acute coronary syndrome
Beschreibung

Acute Coronary Syndrome

Datentyp

boolean

Alias
UMLS CUI [1]
C0948089
coronary revascularization less than 6 months
Beschreibung

Coronary revascularisation Recent

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0877341
UMLS CUI [1,2]
C0332185
patients requiring surgical correction of post-mi aneurism
Beschreibung

Aneurysm Post Myocardial Infarction | Requirement Correction Surgical

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0002940
UMLS CUI [1,2]
C0687676
UMLS CUI [1,3]
C0027051
UMLS CUI [2,1]
C1514873
UMLS CUI [2,2]
C1947976
UMLS CUI [2,3]
C0543467
lv wall thickness less than 5 mm in site of possible injection
Beschreibung

Wall of left ventricle Thickness | Site Injection

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0504053
UMLS CUI [1,2]
C1280412
UMLS CUI [2,1]
C1515974
UMLS CUI [2,2]
C1533685
patients with crt implanted within 3 month before cells injection
Beschreibung

Implantation of CRT-D Recent

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1135480
UMLS CUI [1,2]
C0332185
clinically significant associated diseases
Beschreibung

Comorbidity Clinical Significance

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C2826293
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Ähnliche Modelle

Eligibility Heart Failure NCT01354678

1 Formulare
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
Coronary Artery Disease | Heart failure New York Heart Association Classification
Item
patients with coronary artery disease (cad) and hf ii-iii nyha class
boolean
C1956346 (UMLS CUI [1])
C0018801 (UMLS CUI [2,1])
C1275491 (UMLS CUI [2,2])
Myocardial Infarction
Item
mi more than 6 months before the study
boolean
C0027051 (UMLS CUI [1])
Left ventricular ejection fraction
Item
lvef less than 35%
boolean
C0428772 (UMLS CUI [1])
Absence Indication Coronary revascularisation
Item
absence of indication to coronary revascularization
boolean
C0332197 (UMLS CUI [1,1])
C3146298 (UMLS CUI [1,2])
C0877341 (UMLS CUI [1,3])
Pharmacotherapy Optimal
Item
optimal pharmacological therapy no less than 8 weeks
boolean
C0013216 (UMLS CUI [1,1])
C2698651 (UMLS CUI [1,2])
Medical contraindication Heart Transplantation
Item
heart transplantation is contraindicated
boolean
C1301624 (UMLS CUI [1,1])
C0018823 (UMLS CUI [1,2])
Implantable defibrillator | Cardiac Resynchronization Therapy Devices
Item
patients with implantable cardioverter-defibrillator (icd) or cardiac resynchronization therapy defibrillator (crt-d)
boolean
C0162589 (UMLS CUI [1])
C2936377 (UMLS CUI [2])
Informed Consent
Item
patients giving informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Acute Coronary Syndrome
Item
acute coronary syndrome
boolean
C0948089 (UMLS CUI [1])
Coronary revascularisation Recent
Item
coronary revascularization less than 6 months
boolean
C0877341 (UMLS CUI [1,1])
C0332185 (UMLS CUI [1,2])
Aneurysm Post Myocardial Infarction | Requirement Correction Surgical
Item
patients requiring surgical correction of post-mi aneurism
boolean
C0002940 (UMLS CUI [1,1])
C0687676 (UMLS CUI [1,2])
C0027051 (UMLS CUI [1,3])
C1514873 (UMLS CUI [2,1])
C1947976 (UMLS CUI [2,2])
C0543467 (UMLS CUI [2,3])
Wall of left ventricle Thickness | Site Injection
Item
lv wall thickness less than 5 mm in site of possible injection
boolean
C0504053 (UMLS CUI [1,1])
C1280412 (UMLS CUI [1,2])
C1515974 (UMLS CUI [2,1])
C1533685 (UMLS CUI [2,2])
Implantation of CRT-D Recent
Item
patients with crt implanted within 3 month before cells injection
boolean
C1135480 (UMLS CUI [1,1])
C0332185 (UMLS CUI [1,2])
Comorbidity Clinical Significance
Item
clinically significant associated diseases
boolean
C0009488 (UMLS CUI [1,1])
C2826293 (UMLS CUI [1,2])
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